Enzymune-Test TSH

FDA 510(k) K832823 · Icl Scientific

Substantially Equivalent

510(k) numberK832823

Submission

Device name
Enzymune-Test TSH
Applicant
Icl Scientific
Walker, MI, US
Received
August 19, 1983
Decision date
October 14, 1983
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
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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
K162698MAGLUMI 2000 TSH, MAGLUMI 2000 Immunoassay AnalyzerJLW · Traditional Shenzhen New Industries Biomedical Engineering…07/14/2017SE

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K833761Therapeutic Drug ControlDKB · Traditional 01/13/1984SE
K831383Event-Test SlideJHJ · Traditional 06/22/1983SE
K823199Enzyme-Test DigoxinKXT · Traditional 11/29/1982SE
K822777Therapeutic Drug ControlDIF · Traditional 10/08/1982SE
K822346Histimune Enzyme-Ana TestLJM · Traditional 10/08/1982SE
K822465Enzymune System IJJE · Traditional 09/14/1982SE
K821374Enzymune-Test InsulinCFP · Traditional 05/28/1982SE
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Questions and answers

When was Enzymune-Test TSH cleared by the FDA?

Enzymune-Test TSH (K832823) received a 510(k) decision of Substantially Equivalent on October 14, 1983, 56 days after the submission was received.

What is the product code of K832823?

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