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

OPTICOAT T3 EIA KIT

K Number: K981824 · Decision Dec 22, 1998
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
15
Review Days
214

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Basic Information

Device Name
OPTICOAT T3 EIA KIT
K Number
K981824
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biotecx Laboratories, Inc.
Date Received
May 22, 1998
Decision Date
December 22, 1998
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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K883765 TBG 125I RIA KIT, RADIOIMMUNO. OF SERUM THYROXINE
K871211 PROGESTERONE CLASP RADIOIMMUNOASSAY KIT
K863188 HPL RIA KIT
K854876 ALDOSTERONE DIRECT RIA KIT
K851540 ESTRADIOL DIRECT RIA KIT
K844767 RADIOIMMUNOASSAY OF HUMAN SERUM PLASMA OR URINE TO
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