MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM

MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM is an FDA 510(k)-cleared medical device (K913837) manufactured by Vision Medical, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 4, 1991. Regulation: 8.