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FDA 510(k)

RIA TEST KIT SYS. DAMON KIQUISOL FREE

K-Number: K781012 · 1978-07-27

ApplicantDamon Corp.
Decision Date1978-07-27
Product CodeCEC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA TEST KIT SYS. DAMON KIQUISOL FREE is the device name listed in this FDA 510(k) record. The listed applicant is Damon Corp.. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K781012. The device is classified under product code CEC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA TEST KIT SYS. DAMON KIQUISOL FREE?

RIA TEST KIT SYS. DAMON KIQUISOL FREE is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Damon Corp.. The 510(k) number is K781012.

When did RIA TEST KIT SYS. DAMON KIQUISOL FREE receive FDA 510(k) clearance?

RIA TEST KIT SYS. DAMON KIQUISOL FREE received FDA 510(k) clearance on 1978-07-27, under 510(k) number K781012.

Who is the listed applicant for RIA TEST KIT SYS. DAMON KIQUISOL FREE?

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

What is the FDA product code for RIA TEST KIT SYS. DAMON KIQUISOL FREE?

The FDA product code for RIA TEST KIT SYS. DAMON KIQUISOL FREE is CEC.

Related Clinical Trials

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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 KITK790250LIQUISOL CORTISOL RIA TEST KITK782124IEC CENTRA-7 CENTRIFUGE MODEL 2362

View all 11 devices →

Related Devices (Code: CEC)

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.

K240273Access Free T4Beckman Coulter, Inc.K220456Elecsys FT4 IVRoche DiagnosticsK182423MAGLUMI 2000 FT4Shenzhen New Industries Biomedical Engineering Co., Ltd.K181233Elecsys FT4 IIIRoche DiagnosticsK173122Abbott Architect Free T4Abbott LaboratoriesK152422FREND™ Free T4 Test SystemNanoentek USA, Inc.

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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