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FDA 510(k)

USCI INTRALUMINAL GRAFT W/DACRON TIE

K-Number: K801156 · 1980-05-23

ApplicantC.R. Bard, Inc.
Decision Date1980-05-23
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI INTRALUMINAL GRAFT W/DACRON TIE 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 1980-05-23 under 510(k) number K801156. 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 INTRALUMINAL GRAFT W/DACRON TIE?

USCI INTRALUMINAL GRAFT W/DACRON TIE is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K801156.

When did USCI INTRALUMINAL GRAFT W/DACRON TIE receive FDA 510(k) clearance?

USCI INTRALUMINAL GRAFT W/DACRON TIE received FDA 510(k) clearance on 1980-05-23, under 510(k) number K801156.

Who is the listed applicant for USCI INTRALUMINAL GRAFT W/DACRON TIE?

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 INTRALUMINAL GRAFT W/DACRON TIE?

The FDA product code for USCI INTRALUMINAL GRAFT W/DACRON TIE 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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