ALTERNATING PRESSURE AIR FLOTATION MATTRESS

ALTERNATING PRESSURE AIR FLOTATION MATTRESS is an FDA 510(k)-cleared medical device (K972153) manufactured by Decubiti Concepts, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 30, 1997. Regulation: 8.