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FDA 510(k)

TEST SYSTEM, RIA CORTISOL

K-Number: K760256 · 1976-08-11

ApplicantCorning Medical & Scientific
Decision Date1976-08-11
Product CodeCGR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TEST SYSTEM, RIA CORTISOL is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760256. 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 TEST SYSTEM, RIA CORTISOL?

TEST SYSTEM, RIA CORTISOL is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Corning Medical & Scientific. The 510(k) number is K760256.

When did TEST SYSTEM, RIA CORTISOL receive FDA 510(k) clearance?

TEST SYSTEM, RIA CORTISOL received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760256.

Who is the listed applicant for TEST SYSTEM, RIA CORTISOL?

The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEST SYSTEM, RIA CORTISOL?

The FDA product code for TEST SYSTEM, RIA CORTISOL is CGR.

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Other records listing Corning Medical & Scientific as applicant

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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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