Athletis™

76 catalogue numbers from H74939347070250, listed by Boston Scientific Corporation, United States, under Catheter, Angioplasty, Peripheral, Transluminal. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
76catalogue numbers in this listing
52510(k) clearances naming this product code
7recalls on this 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 Athletis™
Listed by Boston Scientific Corporation, United States
FDA product code LIT
Device type Catheter, Angioplasty, Peripheral, Transluminal
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2020-10-07

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
Sizes Catheter length 50 to 135 cm; balloon diameter 4 to 12 mm; balloon length 20 to 100 mm

Catalogue Numbers

Catalogue numbers for Athletis™
Catalogue number Size Status
H74939347070250 Catheter Length 50 cm In distribution
H74939347090270 Balloon Length 20 mm In distribution
H74939347070650 Balloon Diameter 7.0 mm In distribution
H74939347051070 Balloon Diameter 5.0 mm In distribution
H74939347061050 Balloon Diameter 6.0 mm In distribution
H74939347100870 Balloon Diameter 10.0 mm In distribution
H74939347040450 Balloon Length 40 mm In distribution
H74939347080870 Catheter Length 75 cm In distribution
H74939347050470 Balloon Length 40 mm In distribution
H74939347120670 Balloon Diameter 12.0 mm In distribution
H74939347071050 Balloon Diameter 7.0 mm In distribution
H74939347100270 Balloon Diameter 10.0 mm In distribution
H74939347120470 Balloon Length 40 mm In distribution
H74939347060450 Balloon Diameter 6.0 mm In distribution
H74939347070270 Balloon Length 20 mm In distribution
H74939347080270 Balloon Length 20 mm In distribution
H74939347100410 Balloon Length 40 mm In distribution
H74939347040650 Balloon Length 60 mm In distribution
H74939347080410 Catheter Length 135 cm In distribution
H74939347060250 Catheter Length 50 cm In distribution
H74939347080470 Balloon Diameter 8.0 mm In distribution
H74939347050450 Balloon Diameter 5.0 mm In distribution
H74939347080650 Balloon Diameter 8.0 mm In distribution
H74939347050270 Catheter Length 75 cm In distribution
H74939347040470 Balloon Length 40 mm In distribution
H74939347080450 Balloon Diameter 8.0 mm In distribution
H74939347040250 Balloon Length 20 mm In distribution
H74939347070210 Catheter Length 135 cm In distribution
H74939347040670 Balloon Diameter 4.0 mm In distribution
H74939347060670 Balloon Diameter 6.0 mm In distribution
H74939347080210 Balloon Diameter 8.0 mm In distribution
H74939347060650 Balloon Length 60 mm In distribution
H74939347050670 Balloon Diameter 5.0 mm In distribution
H74939347090410 Balloon Length 40 mm In distribution
H74939347050410 Balloon Diameter 5.0 mm In distribution
H74939347071070 Balloon Length 100 mm In distribution
H74939347040270 Balloon Length 20 mm In distribution
H74939347060470 Balloon Length 40 mm In distribution
H74939347120210 Catheter Length 135 cm In distribution
H74939347080250 Balloon Length 20 mm In distribution
H74939347060210 Balloon Length 20 mm In distribution
H74939347081050 Catheter Length 50 cm In distribution
H74939347041070 Balloon Diameter 4.0 mm In distribution
H74939347050870 Balloon Diameter 5.0 mm In distribution
H74939347070670 Balloon Length 60 mm In distribution
H74939347050850 Catheter Length 50 cm In distribution
H74939347060410 Balloon Diameter 6.0 mm In distribution
H74939347081070 Balloon Diameter 8.0 mm In distribution
H74939347070450 Balloon Length 40 mm In distribution
H74939347070850 Balloon Diameter 7.0 mm In distribution
H74939347090250 Balloon Diameter 9.0 mm In distribution
H74939347090850 Balloon Diameter 9.0 mm In distribution
H74939347080850 Catheter Length 50 cm In distribution
H74939347070870 Catheter Length 75 cm In distribution
H74939347070470 Balloon Length 40 mm In distribution
H74939347051050 Balloon Diameter 5.0 mm In distribution
H74939347080670 Catheter Length 75 cm In distribution
H74939347040850 Balloon Length 80 mm In distribution
H74939347090450 Balloon Length 40 mm In distribution
H74939347080370 Balloon Length 30 mm In distribution
H74939347061070 Catheter Length 75 cm In distribution
H74939347100470 Catheter Length 75 cm In distribution
H74939347060870 Catheter Length 75 cm In distribution
H74939347060850 Catheter Length 50 cm In distribution
H74939347040870 Balloon Diameter 4.0 mm In distribution
H74939347060270 Catheter Length 75 cm In distribution
H74939347080350 Balloon Length 30 mm In distribution
H74939347050650 Balloon Diameter 5.0 mm In distribution
H74939347090870 Balloon Diameter 9.0 mm In distribution
H74939347041050 Balloon Length 100 mm In distribution
H74939347070410 Balloon Diameter 7.0 mm In distribution
H74939347120610 Balloon Diameter 12.0 mm In distribution
H74939347120410 Catheter Length 135 cm In distribution
H74939347090470 Balloon Diameter 9.0 mm In distribution
H74939347120270 Balloon Length 20 mm In distribution
H74939347050250 Catheter Length 50 cm 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
K241683 2024-07-10
K201170 2020-09-15
K162350 2016-11-04
K143193 2015-07-24
K150303 2015-06-15
K141150 2014-09-25
K141521 2014-08-21
K141112 2014-07-16
K132810 2014-02-28
K132430 2013-10-17
K113681 2012-01-11
K112697 2011-11-30
K111295 2011-05-31
K103751 2011-03-22
K093636 2009-12-23
K093720 2009-12-23
K092455 2009-09-04
K080982 2008-07-14
K071309 2007-07-13
K071042 2007-06-13
K060959 2006-04-12
K060960 2006-04-12
K052038 2005-08-16
K001134 2000-08-31
K000798 2000-06-08
K992320 2000-05-18
K000570 2000-04-13
K993305 2000-04-10
K972744 1997-12-11
K972357 1997-11-19
K970379 1997-05-01
K960501 1996-04-09
K953569 1995-12-20
K952063 1995-11-14
K953602 1995-10-18
K934191 1993-12-09
K924320 1993-11-10
K923611 1993-11-04
K921254 1992-12-03
K922610 1992-11-18
K924276 1992-11-10
K924047 1992-11-02
K920547 1992-05-06
K913391 1991-11-05
K913689 1991-10-16
K910995 1991-04-09
K911203 1991-04-09
K896520 1991-03-25
K900094 1990-10-31
K897106 1990-10-16
K897124 1990-07-17
K901018 1990-05-30

Recalls

5 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
2025-12-03 Class II Process change control Boston Scientific is initiating the removal of certain batches of Coyote” Over-the-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter devices due to the potential for inflation/deflation difficulty during use 21 units
2014-02-04 Class II Device Design Boston Scientific is initiating this Recall Removal of one lot of the Coyote” OVER-THE-WIRE PTA Balloon Dilatation Catheter and one lot of the Coyote” MONORAIL” PTA Balloon Dilatation Catheter. Boston Scientific has become aware that the ba 35 for both products. 2014-08-04
2014-02-04 Class II Device Design Boston Scientific is initiating this Recall Removal of one lot of the Coyote” OVER-THE-WIRE PTA Balloon Dilatation Catheter and one lot of the Coyote” MONORAIL” PTA Balloon Dilatation Catheter. Boston Scientific has become aware that the ba 35 for both products 2014-08-04
2013-07-31 Class II Process change control Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of Small Peripheral Cutting Balloon (Monorail and Over-the-Wire) Microsurgical Dilatation Devices and Flextome Cutting Balloon (Monorail and Over-the-Wire) Microsurgi 340 2015-01-27
2013-07-31 Class II Process change control Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of Small Peripheral Cutting Balloon (Monorail and Over-the-Wire) Microsurgical Dilatation Devices and Flextome Cutting Balloon (Monorail and Over-the-Wire) Microsurgi 1,331 2015-01-27
2010-02-18 Not classified Packaging Boston Scientific Corporation is conducting a Medical Device Recall Removal of specific lots/batches of the Blue Max and Ultrathin Diamond Balloon Dilatation Catheters. Boston Scientific has determined that, the sterile barrier in the cathe 73 2011-12-10
2005-12-07 Not classified Other The distal shaft of the catheter may separate during withdrawal of the device from the patient. If the shaft separates, the surgical procedure may be prolonged or require more in-depth surgery to physically remove the broken-off shaft from individual qty in US:376, Worldwide distribution pending. 2007-08-10

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