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FDA 510(k)

BARD PTFE VASCULAR PROSTHESIS

K-Number: K821716 · 1982-08-31

ApplicantC.R. Bard, Inc.
Decision Date1982-08-31
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD PTFE VASCULAR PROSTHESIS 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 1982-08-31 under 510(k) number K821716. 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 PROSTHESIS?

BARD PTFE VASCULAR PROSTHESIS is a medical device that received FDA 510(k) clearance on 1982-08-31. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K821716.

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

BARD PTFE VASCULAR PROSTHESIS received FDA 510(k) clearance on 1982-08-31, under 510(k) number K821716.

Who is the listed applicant for BARD PTFE VASCULAR PROSTHESIS?

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 PROSTHESIS?

The FDA product code for BARD PTFE VASCULAR PROSTHESIS 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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