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

AMEDICA DRUG SCREEN PHENCYCLIDINE TEST

K Number: K023109 · Decision Dec 16, 2002
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
87
Applicant Total
13
Review Days
89

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Basic Information

Device Name
AMEDICA DRUG SCREEN PHENCYCLIDINE TEST
K Number
K023109
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Amedica Biotech, Inc.
Date Received
September 18, 2002
Decision Date
December 16, 2002
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

Similar 510(k) Clearances

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

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Other Clearances by Amedica Biotech, Inc.

K Number Device Name
K100108 AMEDICA DRUG TEST THC, COC, OPI, AMP, MET, PCP, BAR, BZO, MDMA, OXY, TCA
K082898 AMEDICA DRUG SCREEN TEST CUP
K080872 AMEDICHECK DRUG SCREEN THC, COC, OPI, AMP, MET, PCP, MDMA,BAR, BZ
K063379 AMEDICA DRUG SCREEN THC, COC, OPI, AMP, MET, PCP, MDMA, BAR, BZO, M, MODELS C1210, C1220
K061556 AMEDICA DRUG SCREEN THC, COC,OPI,AMP,MET,PCP,MDMA,BAR,BZO,; MODEL C1010,C1015,C1020
K040464 AMEDICA DRUG SCREEN THC/COC, OP1300, PPX, OXY, BAR/BZO TEST
K031497 AMEDICA DRUG SCREEN MDMA-BAR-BZO-MTD-TCA TEST
K023104 AMEDICA DRUG SCREEN AMPHETAMINE TEST
K023101 AMEDICA DRUG SCREEN METHAPHETAMINE TEST
K023047 AMEDICA DRUG SCREEN OPIATES TEST
Search all 13 clearances from Amedica Biotech, Inc. →