ValPro 2 Plus, VaPro 2 Plus Pocket

ValPro 2 Plus, VaPro 2 Plus Pocket is an FDA 510(k)-cleared medical device (K183253) 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 December 17, 2018. Regulation: 8.