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FDA 510(k)

CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO.

K-Number: K897026 · 1990-02-26

ApplicantCanyon Medical Products
Decision Date1990-02-26
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO. is the device name listed in this FDA 510(k) record. The listed applicant is Canyon Medical Products. It received FDA 510(k) clearance on 1990-02-26 under 510(k) number K897026. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO.?

CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO. is a medical device that received FDA 510(k) clearance on 1990-02-26. The listed applicant is Canyon Medical Products. The 510(k) number is K897026.

When did CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO. receive FDA 510(k) clearance?

CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO. received FDA 510(k) clearance on 1990-02-26, under 510(k) number K897026.

Who is the listed applicant for CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO.?

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

What is the FDA product code for CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO.?

The FDA product code for CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO. is DWF.

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 Canyon 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.

K954181CANYONS BI-DIRECTIONAL CHECK VALVEK874899CANYON MEDICAL FEMORAL BYPASS CANNULAE

Related Devices (Code: DWF)

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.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, 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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