HYDROTEC LOW AIR LOSS THERAPY BED

HYDROTEC LOW AIR LOSS THERAPY BED is an FDA 510(k)-cleared medical device (K970363) manufactured by Apex Metal, 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 November 16, 1997. Regulation: 8.