PROSYS URIHESICE SYSTEM NL

PROSYS URIHESICE SYSTEM NL is an FDA 510(k)-cleared medical device (K950690) 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 March 22, 1995. Regulation: 8.