PROSYS URIHESIVE SYSTEM LA

PROSYS URIHESIVE SYSTEM LA is an FDA 510(k)-cleared medical device (K951530) manufactured by Convatec, A Division of E.R. Squibb & Sons. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 11, 1995. Regulation: 8.