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

FREE TRIIODOTHYRONINE(FT3) ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM (IN-VITRO DIAGNOSTIC SYSTEM)

K Number: K962355 · Decision Jul 12, 1996
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
143
Applicant Total
96
Review Days
24

Basic Information

Device Name
FREE TRIIODOTHYRONINE(FT3) ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM (IN-VITRO DIAGNOSTIC SYSTEM)
K Number
K962355
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BAYER CORP.
Date Received
June 18, 1996
Decision Date
July 12, 1996
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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