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FDA 510(k)

CENTRIA FSH RIA

K-Number: K792233 · 1980-01-21

ApplicantUnion Carbide Corp.
Decision Date1980-01-21
Product CodeCGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIA FSH 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 1980-01-21 under 510(k) number K792233. The device is classified under product code CGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIA FSH RIA?

CENTRIA FSH RIA is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is Union Carbide Corp.. The 510(k) number is K792233.

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

CENTRIA FSH RIA received FDA 510(k) clearance on 1980-01-21, under 510(k) number K792233.

Who is the listed applicant for CENTRIA FSH 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 FSH RIA?

The FDA product code for CENTRIA FSH RIA is CGJ.

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Other records listing Union Carbide Corp. as applicant

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Related Devices (Code: CGJ)

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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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