Medical Device Manufacturer · US , Warren , NJ

Cordis Corp., A Johnson & Johnson Co. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006

Recent clearances: MICRO GUIDE CATHETER ELITE, ADROIT GUIDING CATHETER, OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cordis Corp., A Johnson & Johnson Co. Cardiovascular ✕

5 devices

1-5 of 5

Cleared Nov 14, 2014

MICRO GUIDE CATHETER ELITE

Cardiovascular · 266d

Cleared May 29, 2013

ADROIT GUIDING CATHETER

Cardiovascular · 29d

Cleared Feb 04, 2010

OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER

Cardiovascular · 296d

Cleared Jan 13, 2009

OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120

Cardiovascular · 22d

Cleared Sep 22, 2006

ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE...

Cardiovascular · 24d