PERSOL, MOSCLHINO, AND GERALD GENTA

PERSOL, MOSCLHINO, AND GERALD GENTA is an FDA 510(k)-cleared medical device (K942845) manufactured by Persol America, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 3, 1994. Regulation: 8.