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FDA 510(k)

VEIN GRAFT CANNULA

K-Number: K791832 · 1979-10-04

ApplicantD/P, Inc.
Decision Date1979-10-04
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VEIN GRAFT CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is D/P, Inc.. It received FDA 510(k) clearance on 1979-10-04 under 510(k) number K791832. 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 VEIN GRAFT CANNULA?

VEIN GRAFT CANNULA is a medical device that received FDA 510(k) clearance on 1979-10-04. The listed applicant is D/P, Inc.. The 510(k) number is K791832.

When did VEIN GRAFT CANNULA receive FDA 510(k) clearance?

VEIN GRAFT CANNULA received FDA 510(k) clearance on 1979-10-04, under 510(k) number K791832.

Who is the listed applicant for VEIN GRAFT CANNULA?

The FDA 510(k) record lists D/P, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VEIN GRAFT CANNULA?

The FDA product code for VEIN GRAFT CANNULA is DWF.

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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.

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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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