Amerlex-M Follicle Stimulating Hormone(Fsh)Radioim

FDA 510(k) K851361 · Amersham Corp.

Substantially Equivalent

510(k) numberK851361

Submission

Device name
Amerlex-M Follicle Stimulating Hormone(Fsh)Radioim
Applicant
Amersham Corp.
Arlington Heights, IL, US
Received
April 4, 1985
Decision date
May 7, 1985
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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Questions and answers

When was Amerlex-M Follicle Stimulating Hormone(Fsh)Radioim cleared by the FDA?

Amerlex-M Follicle Stimulating Hormone(Fsh)Radioim (K851361) received a 510(k) decision of Substantially Equivalent on May 7, 1985, 33 days after the submission was received.

What is the product code of K851361?

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