MATTRESS, AIR FLOATATION, ALTERN. PRESS.

MATTRESS, AIR FLOATATION, ALTERN. PRESS. is an FDA 510(k)-cleared medical device (K803307) manufactured by Intl. Medical Equipment Corp.. 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 January 12, 1981. Regulation: 8.