LITECURE THERAPY SYSTEM MODEL LTS-1500

LITECURE THERAPY SYSTEM MODEL LTS-1500 is an FDA 510(k)-cleared medical device (K123014) manufactured by Litecure, LLC. 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 28, 2013. Regulation: 8.