Versus Catheter (VS110-9NB)— 510(k) K260149
Substantially EquivalentLiquet Medical, Inc.
FDA 510(k) clearance K260149 for Versus Catheter (VS110-9NB), Substantially Equivalent on 2026-02-17. Applicant: Liquet Medical, Inc.. Device class: 2.
Summary
Liquet Medical's Versus Catheter (VS110-9NB) is filed under product code QEY, mechanical thrombolysis catheter. The record doesn't describe the catheter beyond its name and that code name.
Class II, 21 CFR 870.5150. Cardiovascular is both the classification panel and the review panel. It came in as a Special 510(k).
Liquet Medical filed from Glen Allen, Virginia. FDA found it substantially equivalent 28 calendar days after receipt (January 20 to February 17, 2026).
Clearance details
- Applicant
- Liquet Medical, Inc.
- Product code
- Product code QEY
- Device class
- Class 2
- Regulation
- 21 CFR 870.5150
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Glen Allen, VA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.