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FDA 510(k)

CANYON MEDICAL FEMORAL BYPASS CANNULAE

K-Number: K874899 · 1988-02-18

Decision Date1988-02-18
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CANYON MEDICAL FEMORAL BYPASS CANNULAE 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 1988-02-18 under 510(k) number K874899. 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?

CANYON MEDICAL FEMORAL BYPASS CANNULAE is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Canyon Medical Products. The 510(k) number is K874899.

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

CANYON MEDICAL FEMORAL BYPASS CANNULAE received FDA 510(k) clearance on 1988-02-18, under 510(k) number K874899.

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

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?

The FDA product code for CANYON MEDICAL FEMORAL BYPASS CANNULAE 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.

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.

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.

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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