Medical Device Manufacturer · US , Warren , NJ

Cordis Corporation - FDA 510(k) Cleared Devices

13 submissions · 12 cleared · Since 2004

13

Total

12

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cordis Corporation Gastroenterology & Urology ✕

1 devices

1-1 of 1

Cleared Aug 03, 2004

PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Gastroenterology & Urology · 32d