FEMTEC LASER MICROKERATOME

FEMTEC LASER MICROKERATOME is an FDA 510(k)-cleared medical device (K033354) manufactured by 20/10 Perfect Vision Optische Gerate GmbH. 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 February 17, 2004. Regulation: 8.