PULMONEX DYNAMIC AIR THERAPY UNIT

PULMONEX DYNAMIC AIR THERAPY UNIT is an FDA 510(k)-cleared medical device (K950756) manufactured by Hill-Rom, Inc.. 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 29, 1995. Regulation: 8.