BARD E LUMINEXX BILIARY STENT

BARD E LUMINEXX BILIARY STENT is an FDA 510(k)-cleared medical device (K063532) manufactured by Bard Peripheral Vascular, 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 29, 2008. Regulation: 8.