ACT-1 (ANTERIOR CORNEAL TOPOGRAPHER)

ACT-1 (ANTERIOR CORNEAL TOPOGRAPHER) is an FDA 510(k)-cleared medical device (K912740) manufactured by Visionary Systems, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 29, 1991. Regulation: 8.