MEGABEAM ENDOCULAR PROBE

MEGABEAM ENDOCULAR PROBE is an FDA 510(k)-cleared medical device (K935747) manufactured by Ceram Optec, 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 March 31, 1994. Regulation: 8.