Cortisol Radioimmunoassay Kit-Cortctk

FDA 510(k) K830563 · Sorin Biomedica, Fiat, USA, Inc.

Substantially Equivalent

510(k) numberK830563

Submission

Device name
Cortisol Radioimmunoassay Kit-Cortctk
Applicant
Sorin Biomedica, Fiat, USA, Inc.
Mchenry, IL, US
Received
February 23, 1983
Decision date
May 13, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Cortisol Radioimmunoassay Kit-Cortctk cleared by the FDA?

Cortisol Radioimmunoassay Kit-Cortctk (K830563) received a 510(k) decision of Substantially Equivalent on May 13, 1983, 79 days after the submission was received.

What is the product code of K830563?

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