REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS

REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS is an FDA 510(k)-cleared medical device (K022748) manufactured by Medical Device Services. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 8, 2002. Regulation: 8.