M.F.S. LOW AIR LOSS PULSATING BED

M.F.S. LOW AIR LOSS PULSATING BED is an FDA 510(k)-cleared medical device (K893801) manufactured by Medical 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 July 24, 1989. Regulation: 8.