SANITAS WHIRPOOL BATHING SYSTEM

SANITAS WHIRPOOL BATHING SYSTEM is an FDA 510(k)-cleared medical device (K930624) manufactured by Dutton-Lainson 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 June 30, 1994. Regulation: 8.