Amerlex-M Luteinizing Hormone Radioimmuno-Kit

FDA 510(k) K851104 · Amersham Corp.

Substantially Equivalent

510(k) numberK851104

Submission

Device name
Amerlex-M Luteinizing Hormone Radioimmuno-Kit
Applicant
Amersham Corp.
Arlington Heights, IL, US
Received
March 19, 1985
Decision date
April 10, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CEP – Radioimmunoassay, Luteinizing Hormone
Device class
Class I (low risk)
Regulation
21 CFR 862.1485
Specialty
Clinical Chemistry

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Questions and answers

When was Amerlex-M Luteinizing Hormone Radioimmuno-Kit cleared by the FDA?

Amerlex-M Luteinizing Hormone Radioimmuno-Kit (K851104) received a 510(k) decision of Substantially Equivalent on April 10, 1985, 22 days after the submission was received.

What is the product code of K851104?

The FDA product code is CEP – Radioimmunoassay, Luteinizing Hormone, a Class I (low risk) device regulated under 21 CFR 862.1485.