WATERLASE MD TURBO PLUS MODEL 7200XXX

WATERLASE MD TURBO PLUS MODEL 7200XXX is an FDA 510(k)-cleared medical device (K101658) manufactured by Biolase Technology, 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 August 10, 2010. Regulation: 8.