CAUTERY GRASPER/DISSECTOR

CAUTERY GRASPER/DISSECTOR is an FDA 510(k)-cleared medical device (K994019) manufactured by Starion Instruments. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 19, 2000. Regulation: 8.