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

IMMUBEAD T3 ENZYME IMMUNOASSAY KIT

K Number: K872191 · Decision Aug 13, 1987
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
143
Applicant Total
37
Review Days
66

Basic Information

Device Name
IMMUBEAD T3 ENZYME IMMUNOASSAY KIT
K Number
K872191
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
IMMUNOTECH CORP.
Date Received
June 8, 1987
Decision Date
August 13, 1987
Product Code
CDP
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
CDP Radioimmunoassay, Total Triiodothyronine

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Search all 37 clearances from IMMUNOTECH CORP. →