MICROSULIS TISSUE ABLATION SYSTEM

MICROSULIS TISSUE ABLATION SYSTEM is an FDA 510(k)-cleared medical device (K052919) manufactured by Microsulis Americas, 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 January 12, 2006. Regulation: 8.