OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED

OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED is an FDA 510(k)-cleared medical device (K923710) manufactured by Progressive Medical Technology, 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 March 21, 1993. Regulation: 8.