ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES

ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES is an FDA 510(k)-cleared medical device (K090281) manufactured by Accutech Medical Technologies, 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 March 3, 2009. Regulation: 8.