IOTEC TROCAR AND FLEXIBLE CANNULA

IOTEC TROCAR AND FLEXIBLE CANNULA is an FDA 510(k)-cleared medical device (K970888) manufactured by Iotec Industries. 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 8, 1998. Regulation: 8.