AQUA ARK, IMMERSION HYDROBATH

AQUA ARK, IMMERSION HYDROBATH is an FDA 510(k)-cleared medical device (K861218) manufactured by Aqua Ark, 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 April 17, 1986. Regulation: 8.