ACCU-BEAM C02 LASER HANDPIECE

ACCU-BEAM C02 LASER HANDPIECE is an FDA 510(k)-cleared medical device (K945648) manufactured by Tti Medical. 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 23, 1995. Regulation: 8.