STAGE IV, AIR-FLUIDIZE BED

STAGE IV, AIR-FLUIDIZE BED is an FDA 510(k)-cleared medical device (K904008) manufactured by Unique Flotation Systems, 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 October 9, 1990. Regulation: 8.