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FDA 510(k)

BUHLMANN ANGIOSTENSIN II RIA

K-Number: K954299 · 1995-10-19

ApplicantBuhlmann Laboratories AG
Decision Date1995-10-19
Product CodeCIB
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BUHLMANN ANGIOSTENSIN II RIA is the device name listed in this FDA 510(k) record. The listed applicant is Buhlmann Laboratories AG. It received FDA 510(k) clearance on 1995-10-19 under 510(k) number K954299. The device is classified under product code CIB. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUHLMANN ANGIOSTENSIN II RIA?

BUHLMANN ANGIOSTENSIN II RIA is a medical device that received FDA 510(k) clearance on 1995-10-19. The listed applicant is Buhlmann Laboratories AG. The 510(k) number is K954299.

When did BUHLMANN ANGIOSTENSIN II RIA receive FDA 510(k) clearance?

BUHLMANN ANGIOSTENSIN II RIA received FDA 510(k) clearance on 1995-10-19, under 510(k) number K954299.

Who is the listed applicant for BUHLMANN ANGIOSTENSIN II RIA?

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

What is the FDA product code for BUHLMANN ANGIOSTENSIN II RIA?

The FDA product code for BUHLMANN ANGIOSTENSIN II RIA is CIB.

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Other records listing Buhlmann Laboratories AG as applicant

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Related Devices (Code: CIB)

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.

K123763IDS ISYS DIRECT RENIN ASSAY, IDS ISYS DIRECT RENIN CONTROL SET, AND IDS ISYS DIRECT RENIN CALIBRATION VERIFIERSImmunodiagnostic Systems , Ltd.K121944LIAISON DIRECT RENIN LIAISON CONTROL DIRECT RENIN LIAISON ENDOCRINOLOGY DILUENTDiaSorin, Inc.K062120CISBIO RENIN RIA TESTCis Bio InternationalK061758ACTIVE RENIN IRMADiagnostic Systems Laboratories, Inc.K011128NICHOLS ADVANTAGE DIRECT RENIN (CALIBRATORS, CALIBRATION VERIFIERS, CONTROLS, AND SAMPLE DILUENT)Nichols Institute DiagnosticsK981607ACTIVE RENIN IRMA MODEL NUMBER DSL-25100Diagnostic Systems Laboratories, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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