DIOMED 15 PLUS AND DIOMED 30PLUS LASERS

DIOMED 15 PLUS AND DIOMED 30PLUS LASERS is an FDA 510(k)-cleared medical device (K013499) manufactured by Diomed, 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 November 15, 2001. Regulation: 8.