NC Emerge®

144 catalogue numbers from H7493926820350, listed by Boston Scientific Corporation, United States, under Catheters, Transluminal Coronary Angioplasty, Percutaneous. 12 manufacturers in China are registered for this product code.

Registry build 21.09.26
12manufacturers in China registered for this device type
144catalogue numbers in this listing
10510(k) clearances naming this product code
7recalls on this code

Who Else Makes It

Concentrated in Jiangsu (4), Guangdong (3), Beijing (2).

Chinese manufacturers registered for FDA product code LOX
Manufacturer City Province Registered as Device types
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Lepu Medical Technology (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Beijing Target Medical Technologies Inc. Beijing Beijing Contract manufacturer 7
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Brosmed Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Dongguan TT Medical, Inc. Dongguan Guangdong Manufacturer 4
Kossel Medtech (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 4
Shanghai Microport Medical (Group) Co., Ltd. Shanghai Shanghai Specification developer 1
Sino Medical Sciences Technology Inc. Tianjin Tianjin Manufacturer 1

Record

Regulatory record for NC Emerge®
Listed by Boston Scientific Corporation, United States
FDA product code LOX
Device type Catheters, Transluminal Coronary Angioplasty, Percutaneous
Device class Class 2
Regulation 21 CFR 870.5100
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-24
Record revised 2019-10-07 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for NC Emerge®
Catalogue number Size Status
H7493926820350 3.50 mm Diameter In distribution
H7493926806320 3.25 mm Diameter In distribution
H7493926812600 6.00 mm Diameter In distribution
H7493926712350 3.50 mm Diameter In distribution
H7493926706200 2.00 mm Diameter In distribution
H7493926830350 30 mm Length In distribution
H7493926815300 3.00 mm Diameter In distribution
H7493926812450 4.50 mm Diameter In distribution
H7493926808300 8 mm Length In distribution
H7493926808200 2.00 mm Diameter In distribution
H7493926808370 3.75 mm Diameter In distribution
H7493926830370 30 mm Length In distribution
H7493926708220 2.25 mm Diameter In distribution
H7493926715500 5.00 mm Diameter In distribution
H7493926820370 20 mm Length In distribution
H7493926830320 30 mm Length In distribution
H7493926808320 8 mm Length In distribution
H7493926712270 2.75 mm Diameter In distribution
H7493926812270 12 mm Length In distribution
H7493926808270 8 mm Length In distribution
H7493926806250 2.50 mm Diameter In distribution
H7493926730270 30 mm Length In distribution
H7493926815200 2.00 mm Diameter In distribution
H7493926708300 8 mm Length In distribution
H7493926730320 30 mm Length In distribution
H7493926806400 4.00 mm Diameter In distribution
H7493926820500 20 mm Length In distribution
H7493926712370 3.75 mm Diameter In distribution
H7493926812250 12 mm Length In distribution
H7493926715370 15 mm Length In distribution
H7493926720500 5.00 mm Diameter In distribution
H7493926708270 8 mm Length In distribution
H7493926830400 4.00 mm Diameter In distribution
H7493926720300 3.00 mm Diameter In distribution
H7493926820270 20 mm Length In distribution
H7493926708450 8 mm Length In distribution
H7493926720270 20 mm Length In distribution
H7493926712320 3.25 mm Diameter In distribution
H7493926820200 2.00 mm Diameter In distribution
H7493926812350 3.50 mm Diameter In distribution
H7493926820400 20 mm Length In distribution
H7493926708370 8 mm Length In distribution
H7493926830220 30 mm Length In distribution
H7493926706320 3.25 mm Diameter In distribution
H7493926815550 15 mm Length In distribution
H7493926806200 6 mm Length In distribution
H7493926706270 6 mm Length In distribution
H7493926706450 6 mm Length In distribution
H7493926708200 8 mm Length In distribution
H7493926712400 4.00 mm Diameter In distribution
H7493926730350 30 mm Length In distribution
H7493926820300 3.00 mm Diameter In distribution
H7493926815400 4.00 mm Diameter In distribution
H7493926715200 2.00 mm Diameter In distribution
H7493926715300 3.00 mm Diameter In distribution
H7493926730220 2.25 mm Diameter In distribution
H7493926808400 4.00 mm Diameter In distribution
H7493926712500 12 mm Length In distribution
H7493926715220 2.25 mm Diameter In distribution
H7493926806350 3.50 mm Diameter In distribution
H7493926706250 6 mm Length In distribution
H7493926815450 15 mm Length In distribution
H7493926712450 4.50 mm Diameter In distribution
H7493926712600 6.00 mm Diameter In distribution
H7493926706300 6 mm Length In distribution
H7493926820220 20 mm Length In distribution
H7493926715350 15 mm Length In distribution
H7493926830250 2.50 mm Diameter In distribution
H7493926715450 4.50 mm Diameter In distribution
H7493926706370 6 mm Length In distribution
H7493926812320 3.25 mm Diameter In distribution
H7493926720200 2.00 mm Diameter In distribution
H7493926706500 6 mm Length In distribution
H7493926730370 30 mm Length In distribution
H7493926820550 5.50 mm Diameter In distribution
H7493926720220 20 mm Length In distribution
H7493926712550 12 mm Length In distribution
H7493926815320 3.25 mm Diameter In distribution
H7493926715550 5.50 mm Diameter In distribution
H7493926806270 6 mm Length In distribution
H7493926808550 5.50 mm Diameter In distribution
H7493926808600 6.00 mm Diameter In distribution
H7493926708500 8 mm Length In distribution
H7493926706350 6 mm Length In distribution
H7493926715320 15 mm Length In distribution
H7493926830270 2.75 mm Diameter In distribution
H7493926720450 4.50 mm Diameter In distribution
H7493926815220 2.25 mm Diameter In distribution
H7493926720350 20 mm Length In distribution
H7493926812200 2.00 mm Diameter In distribution
H7493926715400 15 mm Length In distribution
H7493926712220 2.25 mm Diameter In distribution
H7493926812220 2.25 mm Diameter In distribution
H7493926720550 5.50 mm Diameter In distribution
H7493926706220 2.25 mm Diameter In distribution
H7493926808450 4.50 mm Diameter In distribution
H7493926708600 8 mm Length In distribution
H7493926706400 4.00 mm Diameter In distribution
H7493926708400 8 mm Length In distribution
H7493926815270 2.75 mm Diameter In distribution
H7493926806500 5.00 mm Diameter In distribution
H7493926830300 3.00 mm Diameter In distribution
H7493926806300 3.00 mm Diameter In distribution
H7493926812370 3.75 mm Diameter In distribution
H7493926708250 8 mm Length In distribution
H7493926720370 20 mm Length In distribution
H7493926720600 20 mm Length In distribution
H7493926708550 8 mm Length In distribution
H7493926712250 12 mm Length In distribution
H7493926808250 2.50 mm Diameter In distribution
H7493926708320 8 mm Length In distribution
H7493926820250 20 mm Length In distribution
H7493926720250 2.50 mm Diameter In distribution
H7493926815600 15 mm Length In distribution
H7493926715270 15 mm Length In distribution
H7493926812500 5.00 mm Diameter In distribution
H7493926715250 15 mm Length In distribution
H7493926730200 2.00 mm Diameter In distribution
H7493926715600 6.00 mm Diameter In distribution
H7493926808500 5.00 mm Diameter In distribution
H7493926815350 15 mm Length In distribution
H7493926815500 15 mm Length In distribution
H7493926815370 15 mm Length In distribution
H7493926806450 4.50 mm Diameter In distribution
H7493926812550 5.50 mm Diameter In distribution
H7493926720400 20 mm Length In distribution
H7493926730300 3.00 mm Diameter In distribution
H7493926812400 12 mm Length In distribution
H7493926708350 8 mm Length In distribution
H7493926806220 6 mm Length In distribution
H7493926808350 3.50 mm Diameter In distribution
H7493926712300 12 mm Length In distribution
H7493926806370 3.75 mm Diameter In distribution
H7493926830200 2.00 mm Diameter In distribution
H7493926720320 20 mm Length In distribution
H7493926820320 3.25 mm Diameter In distribution
H7493926808220 8 mm Length In distribution
H7493926730250 30 mm Length In distribution
H7493926712200 2.00 mm Diameter In distribution
H7493926820600 20 mm Length In distribution
H7493926815250 15 mm Length In distribution
H7493926730400 30 mm Length In distribution
H7493926820450 20 mm Length In distribution
H7493926812300 3.00 mm Diameter In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sprinter® Legend Medtronic, Inc. 133
NC Quantum Apex™ Boston Scientific Corporation 128
Trek Abbott Vascular 120
Emerge™ Boston Scientific Corporation 119
NC Trek Abbott Vascular 118
Apex™ Boston Scientific Corporation 116
Maverick²™ Boston Scientific Corporation 113
Apollo Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 110
Sprinter® Medtronic, Inc. 108
NC Stormer™ OTW Medtronic, Inc. 108
Quantum™ Maverick™ Boston Scientific Corporation 106
Sapphire NC 24 Coronary Dilatation Catheter OrbusNeich Medical (Shenzhen) Co., Ltd. 98

Showing 12 of 67. All products under Catheters, Transluminal Coronary Angioplasty, Percutaneous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K220629 2022-03-24
K163174 2016-12-14
K163200 2016-12-14
K160823 2016-06-23
K141236 2014-08-07
K134031 2014-07-21
K130391 2013-07-10
K121196 2012-08-31
K121667 2012-08-13
K113220 2012-03-22

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2019-10-24 Class II Process control Certain dilation and extension catheters are being recalled because these catheters may have missed the hydrophilic coating step, which creates a lubricious surface on the devices, during the manufacturing process. 14,145 devices total 2023-03-20
2019-10-24 Class II Process control Certain dilation and extension catheters are being recalled because these catheters may have missed the hydrophilic coating step, which creates a lubricious surface on the devices, during the manufacturing process. 14,145 devices total 2023-03-20
2008-11-21 Not classified Mixed-up of materials/components For one batch/lot of flextome Cutting Balloon (OTW), an incorrect compliance chart was packaged inside the sterile pouch. For the affected batch/lot, the compliance chart packed inside the pouch of the 4.0mm diameter Flextome Cutting Ballo 75 2011-12-10
2006-07-21 Not classified Other Lack of assurance of sterility (pre-sterilization bioburden limits exceeded) 1,000 2007-02-03
2003-08-20 Not classified Other Some of the recalled catheters have a component that has levels of pyrogens above specification. 2 catheters 2005-10-24
2003-08-20 Not classified Other Some of the recalled catheters have a component that has levels of pyrogens above specification. 9 catheters 2005-10-24
2003-08-20 Not classified Other Some of the recalled catheters have a component that has levels of pyrogens above specification. 6 catheters 2005-10-24

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P020037 2003-06-11 FX MINIRAIL RX PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) CATHETER Abbott Vascular
P790017 2003-03-04 NC STORMER OVER-THE-WIRE BALLOON DILATATION CATHETER AND NC STORMER ZIPPER MX BALLOON DILATATION CATHETER Medtronic Ireland
P880027 2002-06-25 PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) Boston Scientific Corporation
P860019 2000-12-08 MAXXUM AND NC MAXXUM PTCA CATHETER Scimed Life Systems, Inc.
P880003 2000-07-07 NINJA FX PTCA DILATATION CATHETER Cordis Corp.
P990008 1999-09-27 COOK MBC PTCA BALLOON DILATATION CATHETER Cook Incorporated
P960014 1998-10-05 MAGELLAN-C PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY(PTCA) CATHETERS MODEL C22020,C22520,C23020,& C23520 Global Therapeutics, Inc.
P970052 1998-04-08 LYNX CONTOUR CORONARY BALLOON DILATATION CATHETER(A NEW MODEL OF THE FACT CATHETER). Endologix LLC
P930012 1997-05-29 THE WRAP(PTCA) CATHETER Progressive Angioplasty Systems, Inc.
P910031 1996-12-02 FACT(TM)AND ARC BALLOON CORNARY DILATATION CATHETERS Abbott Vascular Devices
P890048 1996-11-26 USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS Usci, Div. C.R. Bard, Inc.
P890001 1996-06-07 LEOCOR PICO RUNNER(TM) PTCA CATHETER Leocor, Inc.
P850021 1995-07-12 HYBRID (PTCA) CATHETER Abbott Vascular
P940009 1994-09-29 PERCUTANEUS TRANSLUMINAL CORONARY ANGIOPLASTY CATH Scimed Life Systems, Inc.
P890032 1992-07-23 CORDIS ORION STEERABLE PTCA BALLOON CATHETER Cordis Corp.
P880055 1991-07-19 MICROSS-SL(TM) PTCA DILATATION CATHETER Boston Scientific Corporation
P840040 1991-01-30 HEART TRAK PTCA CATHETER Boston Scientific Corporation
P810046 1990-10-05 ACS RX(R) –.014 CORONARY DILATATION CATHETER Advanced Cardiovascular Systems, Inc.
P870021 1990-10-04 PRIME{TM} MODEL 6520, 6525, 6530 AND 6535 Medtronic, Inc.
P880065 1990-09-19 MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER Boston Scientific Corporation
P870036 1989-06-23 VERSAFLEX BUCHBINDER OMNIFLEX PTCA CATHETER SYSTEM Medtronics Interventional Vascular

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer