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

T3 CLASP-BEAD EIA KIT

K Number: K893620 · Decision Aug 11, 1989
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
15
Review Days
92

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Basic Information

Device Name
T3 CLASP-BEAD EIA KIT
K Number
K893620
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biotecx Laboratories, Inc.
Date Received
May 11, 1989
Decision Date
August 11, 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 Biotecx Laboratories, Inc.

K Number Device Name
K982298 OPTICOAT T4 EIA KIT
K981824 OPTICOAT T3 EIA KIT
K895407 CORTISOL CLASP-BEAD EIA KIT
K892853 T4 CLASP-BEAD EIA KIT
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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