TSH Ria Test System

FDA 510(k) K771222 · Monobind

Substantially Equivalent

510(k) numberK771222

Submission

Device name
TSH Ria Test System
Applicant
Monobind
Mchenry, IL, US
Received
July 5, 1977
Decision date
August 4, 1977
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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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
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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
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More from Shenzhen New Industries Biomedical Engineering Co., Ltd.

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K020548Free T4 (Thytoxine) Microplate Eia Test Models # 1225-300CEC · Traditional 04/05/2002SE
K980088T-Uptake Microplate EiaKHQ · Traditional 02/04/1998SE
K972720Follicle Stimulating Hormone (FSH) Microplate Elisa (425-300)CGJ · Traditional 09/02/1997SE
K971835Anti-Thyroglobulin (TG) Microplate ElisaDDC · Traditional 07/03/1997SE
K971834Anti-Thyroid Peroxidase (Tpo) Microplate ElisaJNL · Traditional 07/03/1997SE
K971921Prolactin (PRL) Hormone Microplate ElisaCFT · Traditional 06/24/1997SE
K971780Thyrotropin(Tsh) ElisaJLW · Traditional 06/24/1997SE

Questions and answers

When was TSH Ria Test System cleared by the FDA?

TSH Ria Test System (K771222) received a 510(k) decision of Substantially Equivalent on August 4, 1977, 30 days after the submission was received.

What is the product code of K771222?

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