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FDA 510(k)

BARD PTFE VASCULAR GRAFT

K-Number: K933204 · 1993-10-27

ApplicantC.R. Bard, Inc.
Decision Date1993-10-27
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD PTFE VASCULAR GRAFT is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1993-10-27 under 510(k) number K933204. The device is classified under product code DSY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD PTFE VASCULAR GRAFT?

BARD PTFE VASCULAR GRAFT is a medical device that received FDA 510(k) clearance on 1993-10-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K933204.

When did BARD PTFE VASCULAR GRAFT receive FDA 510(k) clearance?

BARD PTFE VASCULAR GRAFT received FDA 510(k) clearance on 1993-10-27, under 510(k) number K933204.

Who is the listed applicant for BARD PTFE VASCULAR GRAFT?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD PTFE VASCULAR GRAFT?

The FDA product code for BARD PTFE VASCULAR GRAFT is DSY.

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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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