ENDOFLIP GASTRIC TUBE

ENDOFLIP GASTRIC TUBE is an FDA 510(k)-cleared medical device (K110529) manufactured by Crospon, Ltd.. 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 21, 2011. Regulation: 8.