ELECTRO-KERATOTOME, LINE-OPERATED

ELECTRO-KERATOTOME, LINE-OPERATED is an FDA 510(k)-cleared medical device (K760726) manufactured by Storz Instrument Co.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 4, 1976. Regulation: 8.