SHARP ENDOKNOT PUSHER

SHARP ENDOKNOT PUSHER is an FDA 510(k)-cleared medical device (K914967) manufactured by Sharpe Endosurgical 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 November 21, 1991. Regulation: 8.