DENVER PERITONEO-VENUS SHUNT

DENVER PERITONEO-VENUS SHUNT is an FDA 510(k)-cleared medical device (K894756) manufactured by Codman & Shurtleff, Inc.. 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 September 28, 1989. Regulation: 8.