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

CEDIA DAU METHADONE ASSAY

K Number: K954227 · Decision Nov 17, 1995
Classifications
1
FEI Numbers
93
Registration Numbers
93
Same Product Code
62
Applicant Total
107
Review Days
67

Basic Information

Device Name
CEDIA DAU METHADONE ASSAY
K Number
K954227
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3620
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MICROGENICS CORP.
Date Received
September 11, 1995
Decision Date
November 17, 1995
Product Code
DJR
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
DJR Enzyme Immunoassay, Methadone

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