MODEL 2800 ND:YAG OPHTHALMIC LASER

MODEL 2800 ND:YAG OPHTHALMIC LASER is an FDA 510(k)-cleared medical device (K897099) manufactured by Alcon Surgical, 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 February 15, 1990. Regulation: 8.