CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT

CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT is an FDA 510(k)-cleared medical device (K012090) manufactured by Cordis, A Johnson & Johnson Co.. 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 July 31, 2001. Regulation: 8.