Thyroid Stimulating Hormone

FDA 510(k) K780015 · Pcl-Ria, Inc.

Substantially Equivalent

510(k) numberK780015

Submission

Device name
Thyroid Stimulating Hormone
Applicant
Pcl-Ria, Inc.
Mchenry, IL, US
Received
January 3, 1978
Decision date
February 7, 1978
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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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.

510(k)DeviceDecision
K830526B-Gcg System by RiaJHI · Traditional 04/05/1983SE
K823014Digoxin KitDPB · Traditional 11/01/1982SE
K822935Thyroid Stimulating HormoneJLW · Traditional 11/01/1982SE
K822612T3 Uptake KitsKHQ · Traditional 09/30/1982SE
K820886Thyroxine T4 KitCDX · Traditional 04/16/1982SE
K820358Follicle Stimulating Hormone KitCGJ · Traditional 03/26/1982SE
K820357Luteinizing Hormone KitCEP · Traditional 03/25/1982SE
K812666Thyroxine (T4) 125ICDP · Traditional 10/02/1981SE
K810867Follicle Stimulating Hormone (FSH)JIS · Traditional 04/14/1981SE
K810852Follicle Stimulating Hormone AntiserumCGJ · Traditional 04/08/1981SE

Questions and answers

When was Thyroid Stimulating Hormone cleared by the FDA?

Thyroid Stimulating Hormone (K780015) received a 510(k) decision of Substantially Equivalent on February 7, 1978, 35 days after the submission was received.

What is the product code of K780015?

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