Medical Device Manufacturer · US , Wilmington , DE

The DU Pont Co. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1988

13

Total

13

Cleared

0

Denied

FDA 510(k) Regulatory Record - The DU Pont Co. Gastroenterology & Urology ✕

1 devices

1-1 of 1

Cleared Mar 20, 1990

LABELING CHANGE - VIASPAN(TM) (BELZER UW)

Gastroenterology & Urology · 46d