Versus™ Catheter (VS110-9NB)

Versus™ Catheter (VS110-9NB) is an FDA 510(k)-cleared medical device (K260149) manufactured by Liquet Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 16, 2026. Regulation: 8.