ADVIA Centaur Anti-Thyroglobulin II (aTgII)

FDA 510(k) K250816 · Siemens Healthcare Diagnostics, Inc.

Substantially Equivalent

510(k) numberK250816

Submission

Device name
ADVIA Centaur Anti-Thyroglobulin II (aTgII)
Applicant
Siemens Healthcare Diagnostics, Inc.
Tarrytown, NJ, US
Received
March 18, 2025
Decision date
December 4, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JNL – Immunochemical, Thyroglobulin Autoantibody
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5870
Specialty
Immunology

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K971834Anti-Thyroid Peroxidase (Tpo) Microplate ElisaJNL · Traditional Monobind07/03/1997SE
K962451Hy-Tec/Manual Autoimmune Kit for Thyroid Microsomal (Tpo)JNL · Traditional Hycor Biomedical, Inc.11/25/1996SE
K962341Hy-Tec/Manual Autoimmune Kit for Thyroglobulin (TG)JNL · Traditional Hycor Biomedical, Inc.11/25/1996SE
K954256Anti-TpoJNL · Traditional Biomerica, Inc.11/27/1995SE
K951364Microsomal Eia Test KitJNL · Traditional Immunoprobe, Inc.11/20/1995SE
K951362Thyroglobulin Eia Test KitJNL · Traditional Immunoprobe, Inc.11/20/1995SE

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Questions and answers

When was ADVIA Centaur Anti-Thyroglobulin II (aTgII) cleared by the FDA?

ADVIA Centaur Anti-Thyroglobulin II (aTgII) (K250816) received a 510(k) decision of Substantially Equivalent on December 4, 2025, 261 days after the submission was received.

What is the product code of K250816?

The FDA product code is JNL – Immunochemical, Thyroglobulin Autoantibody, a Class II (moderate risk) device regulated under 21 CFR 866.5870.