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. Radiology ✕

3 devices

1-3 of 3

Cleared Oct 07, 1995

CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGING

Radiology · 75d

Cleared Oct 07, 1995

MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING

Radiology · 75d

Cleared Jul 13, 1995

CRONEX LOW ABSORPTION CASSETTE

Radiology · 20d