Medical Device Manufacturer · US , Wilmington , DE

Dupont Medical Products - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1991

28

Total

28

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dupont Medical Products Toxicology ✕

4 devices

1-4 of 4

Cleared Jun 23, 1995

DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL

Toxicology · 31d

Cleared Dec 28, 1994

PHENOBARBITAL FLEX REAGENT CARTRIDGE

Toxicology · 83d

Cleared Oct 20, 1994

DUPONT ACA PLUS LUTEINIZING HORMONE (LH) METHOD

Toxicology · 65d

Cleared Nov 15, 1993

ACA(R) DIGOXIN ANALYTICAL TEST PACK (DGN)

Toxicology · 161d