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

AMEDICA DRUG SCREEN THC, COC,OPI,AMP,MET,PCP,MDMA,BAR,BZO,; MODEL C1010,C1015,C1020

K Number: K061556 · Decision Jul 21, 2006
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
149
Applicant Total
13
Review Days
46

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Basic Information

Device Name
AMEDICA DRUG SCREEN THC, COC,OPI,AMP,MET,PCP,MDMA,BAR,BZO,; MODEL C1010,C1015,C1020
K Number
K061556
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
862.3870
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Amedica Biotech, Inc.
Date Received
June 5, 2006
Decision Date
July 21, 2006
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

Similar 510(k) Clearances

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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
K040464 AMEDICA DRUG SCREEN THC/COC, OP1300, PPX, OXY, BAR/BZO TEST
K031497 AMEDICA DRUG SCREEN MDMA-BAR-BZO-MTD-TCA TEST
K023109 AMEDICA DRUG SCREEN PHENCYCLIDINE 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. →