Gammadab [125] FSH Radioimmunay Kit

FDA 510(k) K821611 · Clinical Assays, Inc.

Substantially Equivalent

510(k) numberK821611

Submission

Device name
Gammadab [125] FSH Radioimmunay Kit
Applicant
Clinical Assays, Inc.
Mchenry, IL, US
Received
June 2, 1982
Decision date
June 24, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CGJ – Radioimmunoassay, Follicle-Stimulating Hormone
Device class
Class I (low risk)
Regulation
21 CFR 862.1300
Specialty
Clinical Chemistry

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K972720Follicle Stimulating Hormone (FSH) Microplate Elisa (425-300)CGJ · Traditional Monobind09/02/1997SE
K970085Sealite Sciences Aqualite FSHCGJ · Traditional Sealite Sciences, Inc.02/14/1997SE
K964720Vitros Immunodiagnostics Products FSH Reagent Pack (Gem. 1005) FSH Calibrators (GEM.C005)CGJ · Traditional Johnson & Johnson Clinical Diagnostics, Inc.02/04/1997SE
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More from Boehringer Mannheim Corp.

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K832712Folate Radioassay Kit CA-1562-125CGN · Traditional 10/04/1983SE
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K832710Vitamin B12 Radioassay Kit CA-1534CDD · Traditional 10/04/1983SE
K823476Gammadab LH Radio-Kit #CA-1508CEP · Traditional 12/28/1982SE
K823313In Vitro Gammacoat B-Hcg Radio. TestJHI · Traditional 12/22/1982SE
K821092GAMMADAB[125]EGE Radioimmunoassay ItDGC · Traditional 06/22/1982SE
K812227Gammacoat (125) Insulin RadioimmunoassayCFP · Traditional 09/24/1981SE
K810722Gastrin Radioimmunoassay TestCGC · Traditional 05/27/1981SE
K810967In-Vitro TBG Radioimmunoassay TestCEE · Traditional 04/23/1981SE
K801667Gamma COAT(125 I) Rubella AntibodyGOL · Traditional 10/23/1980SE

Questions and answers

When was Gammadab [125] FSH Radioimmunay Kit cleared by the FDA?

Gammadab [125] FSH Radioimmunay Kit (K821611) received a 510(k) decision of Substantially Equivalent on June 24, 1982, 22 days after the submission was received.

What is the product code of K821611?

The FDA product code is CGJ – Radioimmunoassay, Follicle-Stimulating Hormone, a Class I (low risk) device regulated under 21 CFR 862.1300.