Medical Device Manufacturer · US , Mchenry , IL

E.I. Dupont DE Nemours & Co., Inc. - FDA 510(k) Cleared Devices

253 submissions · 252 cleared · Since 1976

253

Total

252

Cleared

0

Denied

FDA 510(k) Regulatory Record - E.I. Dupont DE Nemours & Co., Inc. Toxicology ✕

95 devices

1-12 of 95

Cleared Jun 01, 1995

DUPONT ACA DIGOXIN (DGN A) METHOD

Toxicology · 64d

Cleared Apr 13, 1995

URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGE

Toxicology · 90d

Cleared Apr 05, 1995

URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGE

Toxicology · 82d

Cleared Apr 05, 1995

URINE CANNABINOIDS SCREEN FLEX(TM) REAGENT CARTRIDGE

Toxicology · 78d

Cleared Mar 30, 1995

URINE AMPHETAMINES SCREEN FLEX(TM) REAGENT CARTRIDGE

Toxicology · 76d

Cleared Mar 21, 1995

URINE COCAINE METABOLITE SCREEN FLEX(TM) REAGENT CATRIDGE

Toxicology · 67d

Cleared Mar 21, 1995

URINE METHADONE SCREEN FLEX(TM) REAGENT CARTRIDGE

Toxicology · 63d

Cleared Mar 21, 1995

URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE

Toxicology · 47d

Cleared Mar 20, 1995

URINE PHENCYCLIDINE SCREEN FLEX(TM) REAGENT CARTRIDGE

Toxicology · 62d

Cleared Mar 15, 1995

DUPONT DIMENSION(R) PSEUDOCHOLINESTERASE METHOD

Toxicology · 57d

Cleared Feb 22, 1995

DIGOXIN FLEX(TM) REAGENT CARTRIDGE

Toxicology · 68d

Cleared Feb 22, 1995

DRUGS OF ABUSE CONTROLS

Toxicology · 40d

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