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FDA 510(k)

USCI SAUVAGE EXS VASCULAR PROSTHESIS

K-Number: K800149 · 1980-02-28

ApplicantC.R. Bard, Inc.
Decision Date1980-02-28
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI SAUVAGE EXS 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 1980-02-28 under 510(k) number K800149. 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 USCI SAUVAGE EXS VASCULAR PROSTHESIS?

USCI SAUVAGE EXS VASCULAR PROSTHESIS is a medical device that received FDA 510(k) clearance on 1980-02-28. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K800149.

When did USCI SAUVAGE EXS VASCULAR PROSTHESIS receive FDA 510(k) clearance?

USCI SAUVAGE EXS VASCULAR PROSTHESIS received FDA 510(k) clearance on 1980-02-28, under 510(k) number K800149.

Who is the listed applicant for USCI SAUVAGE EXS 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 USCI SAUVAGE EXS VASCULAR PROSTHESIS?

The FDA product code for USCI SAUVAGE EXS 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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