FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

PHENCYCLIDINE EIA ASSAY

K Number: K935320 · Decision Dec 29, 1993
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
87
Applicant Total
66
Review Days
76

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Basic Information

Device Name
PHENCYCLIDINE EIA ASSAY
K Number
K935320
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Diagnostic Reagents, Inc.
Date Received
October 14, 1993
Decision Date
December 29, 1993
Product Code
LCM
Advisory Committee
Unknown
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
LCM Enzyme Immunoassay, Phencyclidine

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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. →