DISSECTOR, TROUTMAN CORNEAL

DISSECTOR, TROUTMAN CORNEAL is an FDA 510(k)-cleared medical device (K760186) manufactured by V. Mueller O.V. Baxter Healthcare Corp.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 3, 1976. Regulation: 8.