E.I. Dupont DE Nemours & Co., Inc. - FDA 510(k) Cleared Devices
253
Total
252
Cleared
0
Denied
E.I. Dupont DE Nemours & Co., Inc. has 252 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 252 cleared submissions from 1976 to 1996.
Browse the FDA 510(k) cleared devices submitted by E.I. Dupont DE Nemours & Co., Inc. Filter by specialty or product code using the sidebar.
253 devices
Cleared
Jul 24, 1996
ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAY
Microbiology
460d
Cleared
Sep 06, 1995
CRONEX RADIATION THERAPY CASSETTE
Radiology
27d
Cleared
Sep 06, 1995
CRONEX RADIATION THERAPY VERIFICATION CASSETTE
Radiology
27d
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
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