NESSY SURESTICK(TM)/STANDARD SURESTICK(TM)

NESSY SURESTICK(TM)/STANDARD SURESTICK(TM) is an FDA 510(k)-cleared medical device (K925130) manufactured by Laserscope. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 17, 1993. Regulation: 8.