FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ANALYSIS SYSTEM, PREP SAMPLE

K Number: K781941 · Decision Jan 3, 1979
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
253
Review Days
44

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Basic Information

Device Name
ANALYSIS SYSTEM, PREP SAMPLE
K Number
K781941
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3350
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
E.I. Dupont DE Nemours & Co., Inc.
Date Received
November 20, 1978
Decision Date
January 3, 1979
Product Code
DOZ
Advisory Committee
Clinical Toxicology
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
DOZ Liquid Chromatography, Diphenylhydantoin

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. →