D.O.R.C. VFI/VFE SYSTEM

D.O.R.C. VFI/VFE SYSTEM is an FDA 510(k)-cleared medical device (K954842) manufactured by Dutch Ophthalmic USA, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 14, 1996. Regulation: 8.