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

CANNABINOID ENZYME IMMUNOASSAY KIT

K Number: K872882 · Decision Nov 3, 1987
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
149
Applicant Total
39
Review Days
104

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Basic Information

Device Name
CANNABINOID ENZYME IMMUNOASSAY KIT
K Number
K872882
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3870
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
General Diagnostics
Date Received
July 22, 1987
Decision Date
November 3, 1987
Product Code
LDJ
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
LDJ Enzyme Immunoassay, Cannabinoids

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Other Clearances by General Diagnostics

K Number Device Name
K882663 BARBITURATE 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 →