FDA 510(k)

BARD GRAFT SIZER

K-Number: K961134 · 1996-06-19

Decision Date1996-06-19

Product CodeDSY

Advisory CommitteeCV

DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

BARD GRAFT SIZER 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 1996-06-19 under 510(k) number K961134. The device is classified under product code DSY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the BARD GRAFT SIZER?

BARD GRAFT SIZER is a medical device that received FDA 510(k) clearance on 1996-06-19. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K961134.

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

BARD GRAFT SIZER received FDA 510(k) clearance on 1996-06-19, under 510(k) number K961134.

Who is the listed applicant for BARD GRAFT SIZER?

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 GRAFT SIZER?

The FDA product code for BARD GRAFT SIZER is DSY.

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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.