ADL 800 ND:YAG LASER SYSTEM FOR INTRAORAL TIS. SUR

ADL 800 ND:YAG LASER SYSTEM FOR INTRAORAL TIS. SUR is an FDA 510(k)-cleared medical device (K920107) manufactured by Sunrise Technologies, 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 March 12, 1992. Regulation: 8.