AQUA-BLANKET HYPER/HYPOHERMIA BLANKET

AQUA-BLANKET HYPER/HYPOHERMIA BLANKET is an FDA 510(k)-cleared medical device (K890852) manufactured by Ati. 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 April 13, 1989. Regulation: 8.