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FDA 510(k)

ENDAB CORTISOL KIT

K-Number: K810192 · 1981-02-06

ApplicantImmunotech Corp.
Decision Date1981-02-06
Product CodeCGR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ENDAB CORTISOL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Immunotech Corp.. It received FDA 510(k) clearance on 1981-02-06 under 510(k) number K810192. 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 ENDAB CORTISOL KIT?

ENDAB CORTISOL KIT is a medical device that received FDA 510(k) clearance on 1981-02-06. The listed applicant is Immunotech Corp.. The 510(k) number is K810192.

When did ENDAB CORTISOL KIT receive FDA 510(k) clearance?

ENDAB CORTISOL KIT received FDA 510(k) clearance on 1981-02-06, under 510(k) number K810192.

Who is the listed applicant for ENDAB CORTISOL KIT?

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

What is the FDA product code for ENDAB CORTISOL KIT?

The FDA product code for ENDAB CORTISOL KIT 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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