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FDA 510(k)

Versus™ Catheter (VS110-9NB)

K-Number: K260149 · 2026-02-17

Decision Date2026-02-17
Product CodeQEY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Versus™ Catheter (VS110-9NB) is a medical device manufactured by Liquet Medical, Inc.. It received FDA 510(k) clearance on 2026-02-17 under approval number K260149. The device is classified under product code QEY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Versus™ Catheter (VS110-9NB)?

Versus™ Catheter (VS110-9NB) is a medical device that received FDA 510(k) clearance on 2026-02-17. It is manufactured by Liquet Medical, Inc.. The 510(k) number is K260149.

When was Versus™ Catheter (VS110-9NB) approved by the FDA?

Versus™ Catheter (VS110-9NB) received FDA 510(k) clearance on 2026-02-17, under approval number K260149.

What company makes Versus™ Catheter (VS110-9NB)?

Versus™ Catheter (VS110-9NB) is manufactured by Liquet Medical, Inc..

What is the FDA product code for Versus™ Catheter (VS110-9NB)?

The FDA product code for Versus™ Catheter (VS110-9NB) is QEY.

Related Clinical Trials

Other Devices by Liquet Medical, Inc.

Related Devices (Code: QEY)

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.