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

AMEDICHECK DRUG SCREEN THC, COC, OPI, AMP, MET, PCP, MDMA,BAR, BZ

K Number: K080872 · Decision Aug 19, 2008
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
149
Applicant Total
13
Review Days
141

Basic Information

Device Name
AMEDICHECK DRUG SCREEN THC, COC, OPI, AMP, MET, PCP, MDMA,BAR, BZ
K Number
K080872
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
March 31, 2008
Decision Date
August 19, 2008
Product Code
LDJ
Advisory Committee
Clinical Toxicology
Review Advisory Committee
CH
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

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

View all

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
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
K023109 AMEDICA DRUG SCREEN PHENCYCLIDINE TEST
K023101 AMEDICA DRUG SCREEN METHAPHETAMINE TEST
K022954 AMEDICA DRUG SCREEN COCAINE TEST
Search all 13 clearances from AMEDICA BIOTECH, INC. →