SABERX.014 PTA Dilatation Catheter

PTA, RX, 4.0 x 150, 200cm

Registry build 21.09.26
5manufacturers in China registered for this device type
66catalogue numbers in this listing
30510(k) clearances naming this product code

Who Else Makes It

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

Chinese manufacturers registered for FDA product code LIT
Manufacturer City Province Registered as Device types
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Brosmed Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Kossel Medtech (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 4
DK Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for SABERX.014 PTA Dilatation Catheter
Listed by Cordis Corp., United States
FDA product code LIT
Device type Catheter, Angioplasty, Peripheral, Transluminal
Device class Class 2
Regulation 21 CFR 870.1250
510(k) K221832
Record published 2023-07-05

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 SABERX.014 PTA Dilatation Catheter
Catalogue number Size Status
47525020S In distribution
47550020S In distribution
47520020L In distribution
47550080M In distribution
47540150L In distribution
47540250M In distribution
47560150L In distribution
47560040S In distribution
47540020L In distribution
47540080S In distribution
47540040M In distribution
47515120L In distribution
47535200M In distribution
47525250S In distribution
47550300M In distribution
47560080S In distribution
47515020M In distribution
47560020M In distribution
47540100S In distribution
47520200L In distribution
47530150M In distribution
47515100S In distribution
47550020L In distribution
47535020S In distribution
47535150S In distribution
47540300M In distribution
47560080L In distribution
47540250L In distribution
47550120S In distribution
47530020S In distribution
47540200L In distribution
47525150S In distribution
47520080L In distribution
47525040M In distribution
47520080M In distribution
47535300L In distribution
47515080S In distribution
47540250S In distribution
47515020S In distribution
47515020L In distribution
47560020L In distribution
47550120M In distribution
47550100L In distribution
47530250M In distribution
47540080M In distribution
47530250S In distribution
47535020M In distribution
47520120M In distribution
47520040S In distribution
47540200M In distribution
47525150L In distribution
47530200L In distribution
47512015S In distribution
47550250M In distribution
47540120L In distribution
47530150S In distribution
47560080M In distribution
47525300L In distribution
47560250L In distribution
47560040L In distribution
47535300S In distribution
47535020L In distribution
47535150L In distribution
47515040L In distribution
47540080L In distribution
47560200S In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Parafleet SC 018 PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 1,460
Jade Plus PTA Balloon Dilatation Catheter / Jade Plus 18 OTW OrbusNeich Medical (Shenzhen) Co., Ltd. 832
Jade PTA Balloon Dilatation Catheter OrbusNeich Medical (Shenzhen) Co., Ltd. 667
Parafleet SC 014 PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 572
Minerva PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 504
Advocate Arravasc, Ltd. 441
Ultraverse® 035 PTA Dilatation Catheter Bard Peripheral Vascular, Inc. 361
Polux PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 359
Advance Cook Incorporated 355
Pacific™ Plus Medtronic, Inc. 347
EverCross™ ev3, Inc. 316
Achilles NC PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 297

Showing 12 of 167. All products under Catheter, Angioplasty, Peripheral, Transluminal

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K210626 2021-04-23
K201377 2020-10-09
K201333 2020-09-11
K133843 2014-06-27
K121442 2012-06-14
K112797 2012-05-04
K050645 2005-04-01
K003159 2000-10-30
K992825 1999-09-15
K991811 1999-06-15
K981407 1998-05-20
K971516 1997-07-23
K971579 1997-07-18
K971448 1997-07-03
K971010 1997-06-18
K970620 1997-05-06
K970299 1997-04-24
K963000 1997-02-20
K962945 1996-10-23
K955886 1996-03-11
K950119 1995-05-17
K946052 1995-03-03
K942094 1994-11-01
K940868 1994-07-12
K933236 1993-12-27
K905698 1991-07-09
K894899 1990-01-26
K880612 1988-07-28
K844913 1985-08-20
K812168 1981-08-31

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