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FDA 510(k)

BYPASS LEG POSITIONER

K-Number: K932186 · 1993-06-01

ApplicantVoss Medical Products
Decision Date1993-06-01
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BYPASS LEG POSITIONER is the device name listed in this FDA 510(k) record. The listed applicant is Voss Medical Products. It received FDA 510(k) clearance on 1993-06-01 under 510(k) number K932186. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BYPASS LEG POSITIONER?

BYPASS LEG POSITIONER is a medical device that received FDA 510(k) clearance on 1993-06-01. The listed applicant is Voss Medical Products. The 510(k) number is K932186.

When did BYPASS LEG POSITIONER receive FDA 510(k) clearance?

BYPASS LEG POSITIONER received FDA 510(k) clearance on 1993-06-01, under 510(k) number K932186.

Who is the listed applicant for BYPASS LEG POSITIONER?

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

What is the FDA product code for BYPASS LEG POSITIONER?

The FDA product code for BYPASS LEG POSITIONER is FQO.

Related Clinical Trials

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.

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Other records listing Voss Medical Products 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.

K932187PRONE POSITIONERK896338VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULAK885161VOSS VEIN CLAMPK895369VOSS GRAFT MARKER

Related Devices (Code: FQO)

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.

K240598Maestro System (REF100)Moon SurgicalK221410Maestro PlatformMoon SurgicalK090136STERIS CMAX XLT SURGICAL TABLESTERIS CorporationK972810OPT80 THE TRANSPORTABLE (OPT80)O.P.T. USA, Inc.K971988ALLEN, ULTRA AND SMART SOCKETSAllen Medical Systems, Inc.K971307AMSCO SURGICAL TABLESTERIS Corporation

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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