FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ACA (R) DIGITOXIN CALIBRATOR

K Number: K891093 · Decision Apr 26, 1989
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
253
Review Days
55

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Basic Information

Device Name
ACA (R) DIGITOXIN CALIBRATOR
K Number
K891093
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.5160
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
E.I. Dupont DE Nemours & Co., Inc.
Date Received
March 2, 1989
Decision Date
April 26, 1989
Product Code
DCJ
Advisory Committee
Immunology
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DCJ Beta-Globulin, Antigen, Antiserum, Control

Other Clearances by E.I. Dupont DE Nemours & Co., Inc.

K Number Device Name
K951851 ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAY
K953725 CRONEX RADIATION THERAPY VERIFICATION CASSETTE
K953724 CRONEX RADIATION THERAPY CASSETTE
K951441 DUPONT ACA DIGOXIN (DGN A) METHOD
K950137 URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGE
K950136 URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGE
K950181 URINE CANNABINOIDS SCREEN FLEX(TM) REAGENT CARTRIDGE
K950135 URINE AMPHETAMINES SCREEN FLEX(TM) REAGENT CARTRIDGE
K950182 URINE METHADONE SCREEN FLEX(TM) REAGENT CARTRIDGE
K950134 URINE COCAINE METABOLITE SCREEN FLEX(TM) REAGENT CATRIDGE
Search all 253 clearances from E.I. Dupont DE Nemours & Co., Inc. →