PERCUCATH URINARY CATHETER

PERCUCATH URINARY CATHETER is an FDA 510(k)-cleared medical device (K090262) manufactured by Percuvision, LLC. 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 May 27, 2009. Regulation: 8.