DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM

DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM is an FDA 510(k)-cleared medical device (K014007) manufactured by Guidant Corp.. 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 January 6, 2002. Regulation: 8.