FLEXICAIR LOW AIRLOSS THERAPY UNIT

FLEXICAIR LOW AIRLOSS THERAPY UNIT is an FDA 510(k)-cleared medical device (K920382) manufactured by Support Systems Intl.. 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 April 6, 1992. Regulation: 8.