Luteinizing Hormone (Lh-Irma) Ria Kit

FDA 510(k) K864144 · Immuchem Corp.

Substantially Equivalent

510(k) numberK864144

Submission

Device name
Luteinizing Hormone (Lh-Irma) Ria Kit
Applicant
Immuchem Corp.
Carson, CA, US
Received
October 22, 1986
Decision date
November 24, 1986
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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K822509Covalent Coat Ria KitCFP · Traditional 09/28/1982SE
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Questions and answers

When was Luteinizing Hormone (Lh-Irma) Ria Kit cleared by the FDA?

Luteinizing Hormone (Lh-Irma) Ria Kit (K864144) received a 510(k) decision of Substantially Equivalent on November 24, 1986, 33 days after the submission was received.

What is the product code of K864144?

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