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

CEDIA TOTAL T3 ASSAY

K Number: K904098 · Decision Sep 27, 1990
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
107
Review Days
21

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Basic Information

Device Name
CEDIA TOTAL T3 ASSAY
K Number
K904098
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Microgenics Corp.
Date Received
September 6, 1990
Decision Date
September 27, 1990
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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K101742 THERMO SCIENTIFIC CEDIA COCAINE OFT ASSAY
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K101752 THERMO SCIENTIFIC CEDIA MULTI-DRUG OFT CALIBRATORS
K101746 THERMO SCIENTIFIC CEDIA PHENCYCLIDINE (PCP) OFT ASSAY
K101753 THERMO SCIENTIFIC CEDIA METHAMPHETAMINE OFT ASSAY
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