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

BARBITURATE ENZYME IMMUNOASSAY KIT

K Number: K882663 · Decision Sep 19, 1988
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
99
Applicant Total
39
Review Days
84

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Basic Information

Device Name
BARBITURATE ENZYME IMMUNOASSAY KIT
K Number
K882663
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3150
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
General Diagnostics
Date Received
June 27, 1988
Decision Date
September 19, 1988
Product Code
DIS
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
DIS Enzyme Immunoassay, Barbiturate

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Other Clearances by General Diagnostics

K Number Device Name
K872882 CANNABINOID ENZYME IMMUNOASSAY KIT
K871305 COCAINE METABOLITE ENZYME IMMUNOASSAY KIT
K864993 QUALI. ENZYME IMMUNO. OF BARBITURATES IN URINE
K863877 BENZODIAZEPINE ENZYME IMMUNOASSAY KIT
K842307 GENERAL DIAG. CEFONICID 30MCG ANTIMIC
K841465 GENERAL DIAGNOSTICS PLATELET ANTIBODY
K833709 CEFTIZOXIME 30 MCG ANTIMICROBIAL DISK
K832653 CEFUROXIME 30MCG. SUSCEP DISK
K831179 CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP
K830731 NETILMICIN 30 MCG ANTIMICROBIAL DISK
Search all 39 clearances from General Diagnostics →