Medix Biotech Total T3 Enzyme Immunoassay Test Kit

FDA 510(k) K925436 · Medix Biotech, Inc.

Substantially Equivalent

510(k) numberK925436

Submission

Device name
Medix Biotech Total T3 Enzyme Immunoassay Test Kit
Applicant
Medix Biotech, Inc.
Foster City, CA, US
Received
October 28, 1992
Decision date
December 28, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CDP – Radioimmunoassay, Total Triiodothyronine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1710
Specialty
Clinical Chemistry

Other 510(k)s with product code CDP

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K001607Reprobead T3 Enzyme Immunoassay Reagent Kit (Catalog# 104)CDP · Traditional Repromedix Corp.10/05/2000SE
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K991311Total T3 Enzyme Immunoassay Test Kit, Model BC-1005CDP · Traditional Biocheck, Inc.06/02/1999SE
K991252Aia-Pack FT3 AssayCDP · Traditional Tosoh Medics, Inc.05/11/1999SE
K981824Opticoat T3 Eia KitCDP · Traditional Biotecx Laboratories, Inc.12/22/1998SE
K983439Abbott Architect Free T3CDP · Traditional Abbott Laboratories11/20/1998SE
K983434Abbott Architect Total T3CDP · Traditional Abbott Laboratories11/20/1998SE
K974027Auraflex FT3 150 Test Pack, Auraflex FT3 Calibrator PackCDP · Traditional Alfa Biotech (Uk) , Ltd.02/02/1998SE
K974634Immulite Free T3CDP · Traditional Diagnostic Products Corp.01/02/1998SE
K973966Access Total T3 Reagents on the Access Immunoassay AnalyzerCDP · Traditional Beckman Instruments, Inc.10/31/1997SE

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K921700TSH Enzyme Immunoassay Test Kit Cat. No. KIF4093JLW · Traditional 06/29/1992SE
K920712Medix Biotech Throxine Enzyme Immunoassay Test KitKLI · Traditional 03/27/1992SE
K920345Prolactin Enzyme Immunoassay Test Kit (Modified)CFT · Traditional 03/18/1992SE
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Questions and answers

When was Medix Biotech Total T3 Enzyme Immunoassay Test Kit cleared by the FDA?

Medix Biotech Total T3 Enzyme Immunoassay Test Kit (K925436) received a 510(k) decision of Substantially Equivalent on December 28, 1992, 61 days after the submission was received.

What is the product code of K925436?

The FDA product code is CDP – Radioimmunoassay, Total Triiodothyronine, a Class II (moderate risk) device regulated under 21 CFR 862.1710.