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FDA 510(k)

CENTRIA CORTISOL RIA

K-Number: K780725 · 1978-06-06

ApplicantUnion Carbide Corp.
Decision Date1978-06-06
Product CodeCGR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIA CORTISOL RIA is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1978-06-06 under 510(k) number K780725. The device is classified under product code CGR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIA CORTISOL RIA?

CENTRIA CORTISOL RIA is a medical device that received FDA 510(k) clearance on 1978-06-06. The listed applicant is Union Carbide Corp.. The 510(k) number is K780725.

When did CENTRIA CORTISOL RIA receive FDA 510(k) clearance?

CENTRIA CORTISOL RIA received FDA 510(k) clearance on 1978-06-06, under 510(k) number K780725.

Who is the listed applicant for CENTRIA CORTISOL RIA?

The FDA 510(k) record lists Union Carbide Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRIA CORTISOL RIA?

The FDA product code for CENTRIA CORTISOL RIA is CGR.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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