Ciba Corning Acs Cortisol Immunoassay

FDA 510(k) K945367 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK945367

Submission

Device name
Ciba Corning Acs Cortisol Immunoassay
Applicant
Ciba Corning Diagnostics Corp.
Medfield, MA, US
Received
September 26, 1994
Decision date
May 5, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CGR – Radioimmunoassay, Cortisol
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1205
Specialty
Clinical Chemistry

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Questions and answers

When was Ciba Corning Acs Cortisol Immunoassay cleared by the FDA?

Ciba Corning Acs Cortisol Immunoassay (K945367) received a 510(k) decision of Substantially Equivalent on May 5, 1995, 221 days after the submission was received.

What is the product code of K945367?

The FDA product code is CGR – Radioimmunoassay, Cortisol, a Class II (moderate risk) device regulated under 21 CFR 862.1205.