LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM

LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM is an FDA 510(k)-cleared medical device (K062930) manufactured by Alcon Research, Ltd.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 7, 2006. Regulation: 8.