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

VERDICT THC

K Number: K963516 · Decision Oct 30, 1996
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
149
Applicant Total
7
Review Days
57

Basic Information

Device Name
VERDICT THC
K Number
K963516
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3870
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
EDITEK, INC.
Date Received
September 3, 1996
Decision Date
October 30, 1996
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

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Other Clearances by EDITEK, INC.

K Number Device Name
K963692 VERDICT PCP
K963233 EZ-SCREEN PROFILE
K963529 VERDICT BARBITURATES
K943710 VERDICT COCAINE
K943712 VERDICT OPIATES
K943711 EZ-SCREEN:PCP