RUSCH CANTOR TUBE

RUSCH CANTOR TUBE is an FDA 510(k)-cleared medical device (K010798) manufactured by Rusch Intl.. 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 February 25, 2002. Regulation: 8.