Milenia(Tm) FSH (MKFS1,5)

FDA 510(k) K895005 · Diagnostic Products Corp.

Substantially Equivalent

510(k) numberK895005

Submission

Device name
Milenia(Tm) FSH (MKFS1,5)
Applicant
Diagnostic Products Corp.
Los Angeles, CA, US
Received
August 8, 1989
Decision date
October 31, 1989
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 Milenia(Tm) FSH (MKFS1,5) cleared by the FDA?

Milenia(Tm) FSH (MKFS1,5) (K895005) received a 510(k) decision of Substantially Equivalent on October 31, 1989, 84 days after the submission was received.

What is the product code of K895005?

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