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

CEDIA T4 MAB ASSAY MODIFICATION

K Number: K935880 · Decision Mar 3, 1994
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
85
Applicant Total
107
Review Days
87

Basic Information

Device Name
CEDIA T4 MAB ASSAY MODIFICATION
K Number
K935880
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1700
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MICROGENICS CORP.
Date Received
December 6, 1993
Decision Date
March 3, 1994
Product Code
KLI
Advisory Committee
Clinical Chemistry
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
KLI Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine

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