VIABIL BILIARY ENDOPROSTHESIS

VIABIL BILIARY ENDOPROSTHESIS is an FDA 510(k)-cleared medical device (K014215) manufactured by W. L. Gore & Associates, 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 December 18, 2002. Regulation: 8.