Enzymun Test(R) FSH

FDA 510(k) K900763 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK900763

Submission

Device name
Enzymun Test(R) FSH
Applicant
Boehringer Mannheim Corp.
Indianapolis, IN, US
Received
February 16, 1990
Decision date
March 15, 1990
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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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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Questions and answers

When was Enzymun Test(R) FSH cleared by the FDA?

Enzymun Test(R) FSH (K900763) received a 510(k) decision of Substantially Equivalent on March 15, 1990, 27 days after the submission was received.

What is the product code of K900763?

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