WHIRLPOOL BATH MODEL 2270

WHIRLPOOL BATH MODEL 2270 is an FDA 510(k)-cleared medical device (K771967) manufactured by Dazey Products Co.. 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 October 27, 1977. Regulation: 8.