PLASMALIPO/PLASMA D30 LSER SURGICAL DEVICE

PLASMALIPO/PLASMA D30 LSER SURGICAL DEVICE is an FDA 510(k)-cleared medical device (K100098) manufactured by Jm System Co., Ltd.. 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 August 12, 2010. Regulation: 8.