V-Trend Eia TSH

FDA 510(k) K861918 · V-Tech, Inc.

Substantially Equivalent

510(k) numberK861918

Submission

Device name
V-Trend Eia TSH
Applicant
V-Tech, Inc.
Pomona, CA, US
Received
May 19, 1986
Decision date
July 2, 1986
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
K233050ADVIA Centaur® TSH3-Ultra II (TSH3ULII)JLW · Traditional Siemens Healthcare Diagnostics, Inc.04/04/2024SE
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

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K903937Target(Tm) Hog One StepJHI · Traditional 10/22/1990SE
K890978Target Opiates-RDJG · Traditional 11/17/1989SE
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Questions and answers

When was V-Trend Eia TSH cleared by the FDA?

V-Trend Eia TSH (K861918) received a 510(k) decision of Substantially Equivalent on July 2, 1986, 44 days after the submission was received.

What is the product code of K861918?

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