
Alcon Laboratories, Inc.
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ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM is an FDA 510(k)-cleared medical device (K023249) manufactured by Alcon Laboratories, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 17, 2002. Regulation: 8.