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FDA 510(k)

LIQUISOL CORTISOL RIA TEST KIT

K-Number: K790250 · 1979-04-04

ApplicantDamon Corp.
Decision Date1979-04-04
Product Code
DecisionSubstantially Equivalent

Device Summary

LIQUISOL CORTISOL RIA TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Damon Corp.. It received FDA 510(k) clearance on 1979-04-04 under 510(k) number K790250. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUISOL CORTISOL RIA TEST KIT?

LIQUISOL CORTISOL RIA TEST KIT is a medical device that received FDA 510(k) clearance on 1979-04-04. The listed applicant is Damon Corp.. The 510(k) number is K790250.

When did LIQUISOL CORTISOL RIA TEST KIT receive FDA 510(k) clearance?

LIQUISOL CORTISOL RIA TEST KIT received FDA 510(k) clearance on 1979-04-04, under 510(k) number K790250.

Who is the listed applicant for LIQUISOL CORTISOL RIA TEST KIT?

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

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Other records listing Damon Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K874865DAMON D.E.T.E.C.T IMAGE ENHANCERK831826ADRENOCORTICOTROPIN RADIO-IMMUNOASSAYK820686LIQUISOL PROGESTERONE RADIOIMMUNOK802661LIQUISOL TESTOSTERONE RADIOIMM. TEST KITK782124IEC CENTRA-7 CENTRIFUGE MODEL 2362K781012RIA TEST KIT SYS. DAMON KIQUISOL FREE

View all 11 devices →

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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