TSH Riassay

FDA 510(k) K801691 · Ria Diagnostics

Substantially Equivalent

510(k) numberK801691

Submission

Device name
TSH Riassay
Applicant
Ria Diagnostics
Mchenry, IL, US
Received
July 23, 1980
Decision date
August 27, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JLW – Radioimmunoassay, Thyroid-Stimulating Hormone
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1690
Specialty
Clinical Chemistry

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K234091Maverick Diagnostic System TC1000; Maverick Test Panel A0.B0JLW · Traditional Genalyte, Inc.07/22/2024SE
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K222116Atellica® CI Analyzer, Atellica® IMThyroid Stimulating Hormone 3-Ultra (TSH3-UL)…JLW · Traditional Siemens Healthcare Diagnostics, Inc.07/13/2023SE
K221225Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay AnalyzerJLW · Traditional Beckman Coulter, Inc.11/10/2022SE
K190773Elecsys TSHJLW · Traditional Roche Diagnostics04/16/2019SE
K170232AFIAS TSH-SP, AFIAS TSH-VB, AFIAS-6/SP Analyzer, AFIAS-6/VB AnalyzerJLW · Traditional Boditech Med, Inc.10/13/2017SE
K171103Lumipulse G TSH-III Immunoreaction CartridgesJLW · Traditional Fujirebio Diagnostics,Inc.07/28/2017SE
K162698MAGLUMI 2000 TSH, MAGLUMI 2000 Immunoassay AnalyzerJLW · Traditional Shenzhen New Industries Biomedical Engineering…07/14/2017SE

More from Shenzhen New Industries Biomedical Engineering Co., Ltd.

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K855033T-3 Uptake/RiassayKHQ · Traditional 01/24/1986SE
K854798T-4 RiassayCDX · Traditional 01/15/1986SE
K852537T-3 RiassayCDP · Traditional 08/12/1985SE
K810296Digoxin Ria AssayDON · Traditional 02/19/1981SE
K792062Theophylline RiassayLCA · Traditional 02/25/1980SE
K780012Antithrombin III RiaDDQ · Traditional 01/20/1978SE

Questions and answers

When was TSH Riassay cleared by the FDA?

TSH Riassay (K801691) received a 510(k) decision of Substantially Equivalent on August 27, 1980, 35 days after the submission was received.

What is the product code of K801691?

The FDA product code is JLW – Radioimmunoassay, Thyroid-Stimulating Hormone, a Class II (moderate risk) device regulated under 21 CFR 862.1690.