ASPIRA PERITONEAL DRAINAGE SYSTEM

ASPIRA PERITONEAL DRAINAGE SYSTEM is an FDA 510(k)-cleared medical device (K110396) manufactured by C.R. Bard, 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 May 5, 2011. Regulation: 8.