Elias Tmab

FDA 510(k) K925923 · Elias U.S.A., Inc.

Substantially Equivalent

510(k) numberK925923

Submission

Device name
Elias Tmab
Applicant
Elias U.S.A., Inc.
Osceola, WI, US
Received
November 23, 1992
Decision date
January 14, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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

Other 510(k)s with product code JZO

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K250250ADVIA Centaur Anti-Thyroid Peroxidase IIJZO · Traditional Siemens Healthcare Diagnostics, Inc.10/17/2025SE
K240469Access TPO AntibodyJZO · Traditional Beckman Coulter, Inc.08/09/2024SE
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

More from Diagnostic Hybrids, Inc.

510(k)DeviceDecision
K964385Elias ANA-HEP-2LJM · Traditional 03/06/1997SE
K963291Varelisa Ana (4) ProfileLJM · Traditional 09/30/1996SE
K953873Varelisa Helicobacter Pylori AntibodiesLYR · Traditional 08/30/1996SE
K953587Varelisa Mpo-AncaMOB · Traditional 01/26/1996SE
K953586Varelisa PR3-ANCAMOB · Traditional 01/26/1996SE
K951187Varelisa Cardiolipin Abs ScreenMID · Traditional 10/02/1995SE
K951207Varelisa Histone AntibodiesLJM · Traditional 04/17/1995SE
K951206Varelisa Parietal Cell AntibodiesMLE · Traditional 04/17/1995SE
K951205Varelisa Ana ProfileLJM · Traditional 04/17/1995SE
K951186Varelisa ANA-4 ScreenLJM · Traditional 04/17/1995SE

Questions and answers

When was Elias Tmab cleared by the FDA?

Elias Tmab (K925923) received a 510(k) decision of Substantially Equivalent on January 14, 1993, 52 days after the submission was received.

What is the product code of K925923?

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