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FDA 510(k)

ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY

K-Number: K831826 · 1983-07-18

ApplicantDamon Corp.
Decision Date1983-07-18
Product CodeCKG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Damon Corp.. It received FDA 510(k) clearance on 1983-07-18 under 510(k) number K831826. The device is classified under product code CKG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY?

ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is Damon Corp.. The 510(k) number is K831826.

When did ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY receive FDA 510(k) clearance?

ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY received FDA 510(k) clearance on 1983-07-18, under 510(k) number K831826.

Who is the listed applicant for ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY?

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 ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY?

The FDA product code for ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY is CKG.

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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 ENHANCERK820686LIQUISOL PROGESTERONE RADIOIMMUNOK802661LIQUISOL TESTOSTERONE RADIOIMM. TEST KITK790250LIQUISOL CORTISOL RIA TEST KITK782124IEC CENTRA-7 CENTRIFUGE MODEL 2362K781012RIA TEST KIT SYS. DAMON KIQUISOL FREE

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Related Devices (Code: CKG)

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.

K223867IDS ACTH IIImmunodiagnostic Systems LimitedK111335ST AIA-PACK ACTH, AND ST AIA-PACK ACTH CALIBRATOR SET MODEL 025221 AND 025321Tosoh Bioscience, Inc.K060585ROCHE ELECSYS- ACTH,ACTH CALSET,ACTH CALCHECK,PRECICONTROL ACTHRoche Diagnostics Corp.K050748ACTH IMMUNORADIOMETRIC (IRMA) ASSAY KIT, MODEL 3KG011Scantibodies Laboratory, Inc.K021032ACTH IMMUNORADIOMETRIC (IRMA) DIAGNOSTIC ASSAY KIT, MODEL #3KG100Scantibodies Laboratory, Inc.K002638FUTURE DIAGNOSTICS B.V. STAT-ACTH KITFuture Diagnostics B.V.

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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