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FDA 510(k)

RIA KIT, RIANEN CORTISOL

K-Number: K782110 · 1979-01-26

ApplicantNew England Nuclear
Decision Date1979-01-26
Product CodeCGR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA KIT, RIANEN CORTISOL is the device name listed in this FDA 510(k) record. The listed applicant is New England Nuclear. It received FDA 510(k) clearance on 1979-01-26 under 510(k) number K782110. 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 RIA KIT, RIANEN CORTISOL?

RIA KIT, RIANEN CORTISOL is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is New England Nuclear. The 510(k) number is K782110.

When did RIA KIT, RIANEN CORTISOL receive FDA 510(k) clearance?

RIA KIT, RIANEN CORTISOL received FDA 510(k) clearance on 1979-01-26, under 510(k) number K782110.

Who is the listed applicant for RIA KIT, RIANEN CORTISOL?

The FDA 510(k) record lists New England Nuclear as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIA KIT, RIANEN CORTISOL?

The FDA product code for RIA KIT, RIANEN CORTISOL 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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