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FDA 510(k)

Expro Elite Snare, Sympro Elite Snare

K-Number: K163307 · 2017-03-08

ApplicantVascular Solutions, Inc.
Decision Date2017-03-08
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Expro Elite Snare, Sympro Elite Snare is a medical device manufactured by Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2017-03-08 under approval number K163307. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Expro Elite Snare, Sympro Elite Snare?

Expro Elite Snare, Sympro Elite Snare is a medical device that received FDA 510(k) clearance on 2017-03-08. It is manufactured by Vascular Solutions, Inc.. The 510(k) number is K163307.

When was Expro Elite Snare, Sympro Elite Snare approved by the FDA?

Expro Elite Snare, Sympro Elite Snare received FDA 510(k) clearance on 2017-03-08, under approval number K163307.

What company makes Expro Elite Snare, Sympro Elite Snare?

Expro Elite Snare, Sympro Elite Snare is manufactured by Vascular Solutions, Inc..

What is the FDA product code for Expro Elite Snare, Sympro Elite Snare?

The FDA product code for Expro Elite Snare, Sympro Elite Snare is MMX.

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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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