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. Toxicology ✕

3 devices

1-3 of 3

Cleared Mar 10, 1995

DUPONT ACA VANCOMYCIN (VANC) METHOD

Toxicology · 142d

Cleared Nov 16, 1988

ANALYST THEOPHYLLINE CALIBRATOR

Toxicology · 56d

Cleared Oct 31, 1988

ANALYST THEOPHYLLINE ROTOR

Toxicology · 40d