AIR MASSAGE SYSTEM

AIR MASSAGE SYSTEM is an FDA 510(k)-cleared medical device (K780710) manufactured by Theracom C/O Arent, Fox, Kintner, Plotki. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 8, 1978. Regulation: 8.