Firefighter NC Pro
Firefighter NC Pro is a rapid-exchange coronary angioplasty catheter with a noncompliant balloon near its distal tip. Two radiopaque marker bands beneath the balloon help position it at the…
Firefighter NC Pro is a rapid-exchange coronary angioplasty catheter with a noncompliant balloon near its distal tip. Two radiopaque marker bands beneath the balloon help position it at the treated narrowing.
A hydrophilic coating covers the distal catheter section. The 145 cm catheter accepts guidewires up to 0.014 inches, and balloon dimensions are selected for the vessel and procedure.
Balloon and Guide-Catheter Options
Balloon diameters range from 2.0 to 5.5 mm, with lengths from 6 to 30 mm. The 2.0 to 4.0 mm balloons use a 5 Fr guide catheter, while 4.5 to 5.5 mm balloons require 6 Fr. The post-expansion indication for balloon-expandable stents applies to 2.0 to 5.0 mm models.
12manufacturers in China registered for this device type
59catalogue numbers in this listing
3510(k) clearances naming this product code
Who Else Makes It
Concentrated in Jiangsu (4), Guangdong (3), Beijing (2).
| 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
| Listed by | Shanghai Microport Medical (Group) Co., Ltd., China |
|---|---|
| FDA product code | LOX |
| Device type | Catheters, Transluminal Coronary Angioplasty, Percutaneous |
| Device class | Class 2 |
| Regulation | 21 CFR 870.5100 |
| Establishment | Specification developer, Manufacturer |
| 510(k) | K223189 |
| Record published | 2024-12-18 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Latex | Contains natural rubber latex |
| Label carries | lot or batch number, expiry date, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| SWB5010 | In distribution | |
| SWB3020 | In distribution | |
| SWB3520 | In distribution | |
| SWB4020 | In distribution | |
| SWB3015 | In distribution | |
| SWB3510 | In distribution | |
| SWB2530 | In distribution | |
| SWB4515 | In distribution | |
| SWB4006 | In distribution | |
| SWB4520 | In distribution | |
| SWB2515 | In distribution | |
| SWB3706 | In distribution | |
| SWB2520 | In distribution | |
| SWB3710 | In distribution | |
| SWB2506 | In distribution | |
| SWB2010 | In distribution | |
| SWB3506 | In distribution | |
| SWB2206 | In distribution | |
| SWB2215 | In distribution | |
| SWB2015 | In distribution | |
| SWB4030 | In distribution | |
| SWB5006 | In distribution | |
| SWB5020 | In distribution | |
| SWB2020 | In distribution | |
| SWB2030 | In distribution | |
| SWB2706 | In distribution | |
| SWB2225 | In distribution | |
| SWB4506 | In distribution | |
| SWB2710 | In distribution | |
| SWB3525 | In distribution | |
| SWB5520 | In distribution | |
| SWB2715 | In distribution | |
| SWB4510 | In distribution | |
| SWB2720 | In distribution | |
| SWB3006 | In distribution | |
| SWB2006 | In distribution | |
| SWB5015 | In distribution | |
| SWB4025 | In distribution | |
| SWB4015 | In distribution | |
| SWB5515 | In distribution | |
| SWB3010 | In distribution | |
| SWB2210 | In distribution | |
| SWB2220 | In distribution | |
| SWB2525 | In distribution | |
| SWB2230 | In distribution | |
| SWB3210 | In distribution | |
| SWB3025 | In distribution | |
| SWB4010 | In distribution | |
| SWB5510 | In distribution | |
| SWB3206 | In distribution | |
| SWB2510 | In distribution | |
| SWB3220 | In distribution | |
| SWB3515 | In distribution | |
| SWB3720 | In distribution | |
| SWB3215 | In distribution | |
| SWB3715 | In distribution | |
| SWB2025 | In distribution | |
| SWB3030 | In distribution | |
| SWB3530 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| NC Emerge® | Boston Scientific Corporation | 144 |
| 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 |
Showing 12 of 67. All products under Catheters, Transluminal Coronary Angioplasty, Percutaneous
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K252116 | 2026-04-07 |
| K223189 | 2023-07-21 |
| K143160 | 2015-03-05 |
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.
| 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.