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

AMERLEX T-3 RIA KIT

K Number: K800374 · Decision Mar 12, 1980
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
94
Review Days
20

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Basic Information

Device Name
AMERLEX T-3 RIA KIT
K Number
K800374
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Amersham Corp.
Date Received
February 21, 1980
Decision Date
March 12, 1980
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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K901848 GADOLINIUM-153 BONE DENSITOMETER SOURCES
K901832 GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415
K896270 AMERLITE ESTRADIOL-60 ASSAY LAN.0081/2081
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