ELIOS DIODE OPHTHALMIC LASER

ELIOS DIODE OPHTHALMIC LASER is an FDA 510(k)-cleared medical device (K921320) manufactured by Marco Ophthalmic, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 1, 1992. Regulation: 8.