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

T3 RIA KIT

K Number: K772122 · Decision Nov 17, 1977
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
16
Review Days
7

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Basic Information

Device Name
T3 RIA KIT
K Number
K772122
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Antibodies, Inc.
Date Received
November 10, 1977
Decision Date
November 17, 1977
Product Code
CDP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
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 Antibodies, Inc.

K Number Device Name
K890774 GIARDEIA(TM)
K843590 DETECT-A-STREP
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K812749 ULTRA-DIG
K812314 CRITHIDNA ANTI-DNA TEST KIT
K802877 AMIKACIN RIA KIT
K800743 TOBRAMYCIN RIA KIT
K791217 TSH RIA KIT
K781655 NEPHELRATE ANTISERUMS 1GA
K781654 NEPHELRATE ANTIPERUMS LGM
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