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

MICRO EIA FOR AMPHETAMINE METABOLITES

K Number: K932304 · Decision Dec 7, 1993
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
224
Applicant Total
10
Review Days
209

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Basic Information

Device Name
MICRO EIA FOR AMPHETAMINE METABOLITES
K Number
K932304
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3100
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Microdiagnostics, Inc.
Date Received
May 12, 1993
Decision Date
December 7, 1993
Product Code
DKZ
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
DKZ Enzyme Immunoassay, Amphetamine

Similar 510(k) Clearances

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

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Other Clearances by Microdiagnostics, Inc.

K Number Device Name
K011952 DRUGS OF ABUSE MULTI-TEST STRIP
K991516 MICRO-STRIP FOR MARIJUANA METABOLITES
K991505 MICRO-STRIP FOR PHENCYCLIDINE METABOLITES
K981388 MICRO-STRIP FOR COCAINE METABOLITES
K974611 MICRO-STRIP FOR AMPHETAMINE METABOLITES
K973761 MICRO-STRIP FOR OPIATE METABOLITES
K923468 MICRO EIA FOR OPIATE METABOLITES
K914533 MICRO EIA FOR COCAINE METABOLITES
K914490 MICRO EIA FOR MARIJUANA METABOLITES