ACTITOUCH ACT-ADAPTIVE COMPRESSION THERAPY SYSTEM

ACTITOUCH ACT-ADAPTIVE COMPRESSION THERAPY SYSTEM is an FDA 510(k)-cleared medical device (K131193) manufactured by Tactile Systems Technology, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 17, 2013. Regulation: 8.