FDA 510(k)

MICROFRANCE(R) WORMALD VASCULAR CLAMP

K-Number: K112662 · 2012-01-20

Decision Date2012-01-20

Product CodeDXC

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MICROFRANCE(R) WORMALD VASCULAR CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Xomed, Inc.. It received FDA 510(k) clearance on 2012-01-20 under 510(k) number K112662. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROFRANCE(R) WORMALD VASCULAR CLAMP?

MICROFRANCE(R) WORMALD VASCULAR CLAMP is a medical device that received FDA 510(k) clearance on 2012-01-20. The listed applicant is Medtronic Xomed, Inc.. The 510(k) number is K112662.

When did MICROFRANCE(R) WORMALD VASCULAR CLAMP receive FDA 510(k) clearance?

MICROFRANCE(R) WORMALD VASCULAR CLAMP received FDA 510(k) clearance on 2012-01-20, under 510(k) number K112662.

Who is the listed applicant for MICROFRANCE(R) WORMALD VASCULAR CLAMP?

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

What is the FDA product code for MICROFRANCE(R) WORMALD VASCULAR CLAMP?

The FDA product code for MICROFRANCE(R) WORMALD VASCULAR CLAMP is DXC.

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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.