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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 the device name listed in this FDA 510(k) record. The listed applicant is Sequent Medical, Inc.. It received FDA 510(k) clearance on 2017-02-18 under 510(k) 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. The listed applicant is Sequent Medical, Inc.. The 510(k) number is K162565.

When did VIA 17 Microcatheter receive FDA 510(k) clearance?

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

Who is the listed applicant for VIA 17 Microcatheter?

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

What is the FDA product code for VIA 17 Microcatheter?

The FDA product code for VIA 17 Microcatheter is DQY.

Related Devices (Code: DQY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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