Bayer Diagnostics ACS:180 and Advia Centaur Anti-Tpo Assay

FDA 510(k) K003291 · Bayer Diagnostics Corp.

Substantially Equivalent

510(k) numberK003291

Submission

Device name
Bayer Diagnostics ACS:180 and Advia Centaur Anti-Tpo Assay
Applicant
Bayer Diagnostics Corp.
Medfield, MA, US
Received
October 20, 2000
Decision date
December 5, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JZO – System, Test, Thyroid Autoantibody
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5870
Specialty
Immunology

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K213517Access Thyroglobulin Antibody IIJZO · Traditional Beckman Coulter, Inc.09/26/2023SE
K222610Elecsys Anti-TgJZO · Traditional Roche Diagnostics09/15/2023SE
K193313Elecsys Anti-TSHRJZO · Traditional Roche Diagnostics02/27/2020SE
K151799EliA anti-TG Immunoassay, EliA anti-TPO Immunoassay, EliA Thyroid Positive Control 250…JZO · Traditional Phadia AB03/25/2016SE
K152061IMMULITE 2000 TSI Assay, IMMULITE 2000 TSI Calibration Verification MaterialJZO · Traditional Siemens Healthcare Diagnostics, Inc.03/03/2016SE
K092229Thyretain TM Tsi Reporter BioassayJZO · Traditional Diagnostic Hybrids, Inc.05/18/2010SE
K090760Theratest El-Anti-Tpo and Theratest El-Anti-Thyroglobulin, Model 104-119, 103-120JZO · Traditional Theratest Laboratories, Inc.09/03/2009SE
K083391Thyroid Stimulating Immunoglobulin Reporter AssayJZO · Traditional Diagnostic Hybrids, Inc.05/21/2009SE

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K031857Advia Chemistry ALPHA-1 Antitrypsin AssayDEM · Traditional 09/04/2003SE
K022096Uric Acid Assay for the Advia Integrated Modular SystemKNK · Traditional 03/18/2003SE
K030452Bayer Ligand Plus 1, 2, 3 ControlsJJY · Abbreviated 03/03/2003SE
K023840Acid Phosphatase Assay for the Advia 1650CKB · Traditional 01/07/2003SE
K023841Ammonia Assay for the Advia 1650JIF · Traditional 12/24/2002SE
K022177Prostate Specific Antigen (Psa) Assay for the Advia Integrated Modular SystemLTJ · Traditional 12/17/2002SE
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Questions and answers

When was Bayer Diagnostics ACS:180 and Advia Centaur Anti-Tpo Assay cleared by the FDA?

Bayer Diagnostics ACS:180 and Advia Centaur Anti-Tpo Assay (K003291) received a 510(k) decision of Substantially Equivalent on December 5, 2000, 46 days after the submission was received.

What is the product code of K003291?

The FDA product code is JZO – System, Test, Thyroid Autoantibody, a Class II (moderate risk) device regulated under 21 CFR 866.5870.