Gammadab LH Radio-Kit #CA-1508

FDA 510(k) K823476 · Clinical Assays, Inc.

Substantially Equivalent

510(k) numberK823476

Submission

Device name
Gammadab LH Radio-Kit #CA-1508
Applicant
Clinical Assays, Inc.
Mchenry, IL, US
Received
November 22, 1982
Decision date
December 28, 1982
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 Gammadab LH Radio-Kit #CA-1508 cleared by the FDA?

Gammadab LH Radio-Kit #CA-1508 (K823476) received a 510(k) decision of Substantially Equivalent on December 28, 1982, 36 days after the submission was received.

What is the product code of K823476?

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