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FDA 510(k)

VIA 17 Microcatheter

K-Number: K162565 · 2017-02-18

ApplicantSequent Medical, Inc.
Decision Date2017-02-18
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VIA 17 Microcatheter is a medical device manufactured by Sequent Medical, Inc.. It received FDA 510(k) clearance on 2017-02-18 under approval number K162565. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIA 17 Microcatheter?

VIA 17 Microcatheter is a medical device that received FDA 510(k) clearance on 2017-02-18. It is manufactured by Sequent Medical, Inc.. The 510(k) number is K162565.

When was VIA 17 Microcatheter approved by the FDA?

VIA 17 Microcatheter received FDA 510(k) clearance on 2017-02-18, under approval number K162565.

What company makes VIA 17 Microcatheter?

VIA 17 Microcatheter is manufactured by Sequent Medical, Inc..

What is the FDA product code for VIA 17 Microcatheter?

The FDA product code for VIA 17 Microcatheter is DQY.

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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.

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