ACCU-BEAM FIBER OPTIC HANDPIECE

ACCU-BEAM FIBER OPTIC HANDPIECE is an FDA 510(k)-cleared medical device (K952006) 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 May 30, 1995. Regulation: 8.