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FDA 510(k)

ACTHK-PR RIA KIT

K-Number: K860311 · 1986-04-07

ApplicantCompagnie Oris Industrie, S.A.
Decision Date1986-04-07
Product CodeCKG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACTHK-PR RIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Compagnie Oris Industrie, S.A.. It received FDA 510(k) clearance on 1986-04-07 under 510(k) number K860311. 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 ACTHK-PR RIA KIT?

ACTHK-PR RIA KIT is a medical device that received FDA 510(k) clearance on 1986-04-07. The listed applicant is Compagnie Oris Industrie, S.A.. The 510(k) number is K860311.

When did ACTHK-PR RIA KIT receive FDA 510(k) clearance?

ACTHK-PR RIA KIT received FDA 510(k) clearance on 1986-04-07, under 510(k) number K860311.

Who is the listed applicant for ACTHK-PR RIA KIT?

The FDA 510(k) record lists Compagnie Oris Industrie, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTHK-PR RIA KIT?

The FDA product code for ACTHK-PR RIA KIT is CKG.

Related Clinical Trials

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Other records listing Compagnie Oris Industrie, S.A. 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.

K881323CURIETRON 192 LOW DOSE RATE

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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