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

FREE T3 RADIOIMMUNOASSAY KIT

K Number: K894200 · Decision Sep 25, 1989
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
4
Review Days
101

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Basic Information

Device Name
FREE T3 RADIOIMMUNOASSAY KIT
K Number
K894200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Advanced Magnetics, Inc.
Date Received
June 16, 1989
Decision Date
September 25, 1989
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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Other Clearances by Advanced Magnetics, Inc.

K Number Device Name
K902748 SEROZYME FREE T3 IMMUNOASSAY
K900060 FREE T4 IMMUNOASSAY KIT
K884753 MODIFIED FREE T4 RADIOIMMUNOASSAY KIT