GELPORT BLUNT TIP TROCAR SYSTEM

GELPORT BLUNT TIP TROCAR SYSTEM is an FDA 510(k)-cleared medical device (K060629) manufactured by Applied Medical Resources 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 April 6, 2006. Regulation: 8.