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

CANNABINOID URINE CONTROLS

K Number: K932113 · Decision Jun 29, 1993
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
66
Review Days
57

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Basic Information

Device Name
CANNABINOID URINE CONTROLS
K Number
K932113
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Diagnostic Reagents, Inc.
Date Received
May 3, 1993
Decision Date
June 29, 1993
Product Code
JJX
Advisory Committee
Clinical Chemistry
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JJX), ordered by most recent decision date.

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Other Clearances by Diagnostic Reagents, Inc.

K Number Device Name
K983268 MODIFICATION OF TRICYCLIC SERUM TOX EIA ASSAY
K983812 NAPA EIA ASSAY
K983323 DIGOXIN IMMUNOASSAY
K983280 VANCOMYCIN EIA ASSAY
K983159 DRUGS OF ABUSE URINE CALIBRATORS AND CONTROLS
K973102 LIDOCAINE EIA ASSAY
K972835 50NG/ML COCAINE METABOLITE CALIBRATOR
K972526 METHADONE EIA ASSAY
K964212 QUINIDINE ENZYME IMMUNOASSAY
K963835 DIGOXIN ENZYME IMMUNOASSAY
Search all 66 clearances from Diagnostic Reagents, Inc. →