Elecsys Anti-Tshr Immunoassay, Elecsys Precicontrol Thyroab

FDA 510(k) K080092 · Roche Diagnostics Corp.

Substantially Equivalent

510(k) numberK080092

Submission

Device name
Elecsys Anti-Tshr Immunoassay, Elecsys Precicontrol Thyroab
Applicant
Roche Diagnostics Corp.
Indianapolis, IN, US
Received
January 14, 2008
Decision date
July 28, 2008
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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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
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Questions and answers

When was Elecsys Anti-Tshr Immunoassay, Elecsys Precicontrol Thyroab cleared by the FDA?

Elecsys Anti-Tshr Immunoassay, Elecsys Precicontrol Thyroab (K080092) received a 510(k) decision of Substantially Equivalent on July 28, 2008, 196 days after the submission was received.

What is the product code of K080092?

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