LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS

LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS is an FDA 510(k)-cleared medical device (K122829) manufactured by Lensar, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 2, 2012. Regulation: 8.