VICTUS FEMTOSECOND LASER PLATFORM

VICTUS FEMTOSECOND LASER PLATFORM is an FDA 510(k)-cleared medical device (K122386) manufactured by Technolas Perfect Vision GmbH. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 7, 2013. Regulation: 8.