Liv Pre-lubricated Intermittent Catheter

Liv Pre-lubricated Intermittent Catheter is an FDA 510(k)-cleared medical device (K260502) manufactured by HR Healthcare. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 11, 2026. Regulation: 8.