UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER

UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER is an FDA 510(k)-cleared medical device (K931774) 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 July 21, 1993. Regulation: 8.