E.I. Dupont DE Nemours & Co., Inc. - FDA 510(k) Cleared Devices
Recent clearances: ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAY, CRONEX RADIATION THERAPY CASSETTE, CRONEX RADIATION THERAPY VERIFICATION CASSETTE
253
Total
252
Cleared
0
Denied
FDA 510(k) Regulatory Record - E.I. Dupont DE Nemours & Co., Inc. Hematology ✕
15 devices
Cleared
Aug 20, 1992
DU PONT ACA PLUS IMMUNOASSAY SYSTEM INSTRUMENT
Hematology
77d
Cleared
Feb 16, 1988
L-PHENYLALANINE METHYL ESTER HYDROCHLORIDE PME REA
Hematology
117d
Cleared
Jan 05, 1987
SORVALL CAPSPIN MICROHEMATOCRIT CENTRIFUGE
Hematology
41d
Cleared
Oct 04, 1985
ACA FIBRIN DEGRADATION PROD ANALYTICAL TEST PACK
Hematology
109d
Cleared
Aug 12, 1985
DUPONT ACA FIBRIN OGEN DEGRAD-PRODUCTS CALIBRATOR
Hematology
84d
Cleared
Aug 12, 1985
DUPONT ACA FIBRIN DEGRADATION PROD CLOTTING TUBE
Hematology
56d
Cleared
May 29, 1985
ACA PROTHROMBIN TIME ANALYTICAL TEST PACK
Hematology
71d
Cleared
May 29, 1985
ACA ACTIVATED PARTIAL THROMBOPLASTIN TIME ANALYTIC
Hematology
71d
Cleared
May 29, 1985
DUPONT ACA PROTHROMBIN TIME/ACTIVATED PARTIAL THRO
Hematology
71d
Cleared
Nov 30, 1984
HEPARIN ACA ANALYTICAL TEST PACK
Hematology
108d
Cleared
Nov 30, 1984
HEPARIN CALIBRATOR ACA
Hematology
108d
Cleared
Nov 24, 1981
ACA FIBRINOGEN CALIBRATOR
Hematology
70d
Cleared
Oct 08, 1981
ACA ANTITHROMBIN III TEST PACK
Hematology
23d
Cleared
Oct 08, 1981
ACA FIBRINOGEN TEST PACK
Hematology
24d
Cleared
Mar 31, 1981
ISOLATOR SYSTEM
Hematology
20d