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FDA 510(k)

CENTRIA CORTISOL RIA TEST SET

K-Number: K792243 · 1979-12-06

ApplicantVentrex Laboratories, Inc.
Decision Date1979-12-06
Product CodeCGR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIA CORTISOL RIA TEST SET is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex Laboratories, Inc.. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792243. 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 TEST SET?

CENTRIA CORTISOL RIA TEST SET is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K792243.

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

CENTRIA CORTISOL RIA TEST SET received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792243.

Who is the listed applicant for CENTRIA CORTISOL RIA TEST SET?

The FDA 510(k) record lists Ventrex Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRIA CORTISOL RIA TEST SET?

The FDA product code for CENTRIA CORTISOL RIA TEST SET 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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