VaPro 2 Intermittent Catheter

VaPro 2 Intermittent Catheter is an FDA 510(k)-cleared medical device (K180824) manufactured by Hollister Incorporated. 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 June 21, 2018. Regulation: 8.