URIHESIVE SYSTEM - IMPROVED

URIHESIVE SYSTEM - IMPROVED is an FDA 510(k)-cleared medical device (K834337) manufactured by Convatec, A Division of E.R. Squibb & Sons. 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 February 9, 1984. Regulation: 8.