ACMI DUR-HL LASER SYSTEMS

ACMI DUR-HL LASER SYSTEMS is an FDA 510(k)-cleared medical device (K060752) manufactured by Acmi Corporation. 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 24, 2006. Regulation: 8.