HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES

HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES is an FDA 510(k)-cleared medical device (K844880) manufactured by Huntleigh Technology, 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 January 24, 1985. Regulation: 8.