Versus Catheter (VS110-9NB)— 510(k) K260149

Name: FDA 510(k) clearance K260149
Creator: U.S. Food and Drug Administration
Published: 2026-02-17

Substantially Equivalent

Liquet 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.

Clearance details

Applicant: Liquet Medical, Inc.
Product code: Code QEY
Device class: Class 2
Regulation: 21 CFR 870.5150
Advisory panel: Cardiovascular
Date received: 2026-01-20
Decision date: 2026-02-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Glen Allen, VA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code QEY

view all

K251318 — VariFuse Adjustable Infusion Catheter2026-01-20
K241851 — Versus Catheter (VS110-8B)2024-11-25
K231653 — BASHIR .035 Endovascular Catheter, BASHIR S-B .035 Endovascular Catheter2023-07-03
K222095 — BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 71012023-04-20
K220866 — EKOS+ Endovascular Device2022-04-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.