Ciba Corning Magic Lite LH Immunoassay

FDA 510(k) K902398 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK902398

Submission

Device name
Ciba Corning Magic Lite LH Immunoassay
Applicant
Ciba Corning Diagnostics Corp.
East Walpole, MA, US
Received
May 30, 1990
Decision date
June 28, 1990
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 Ciba Corning Magic Lite LH Immunoassay cleared by the FDA?

Ciba Corning Magic Lite LH Immunoassay (K902398) received a 510(k) decision of Substantially Equivalent on June 28, 1990, 29 days after the submission was received.

What is the product code of K902398?

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