MODEL K210 AND K211 FLUIDOTHERAPY UNITS

MODEL K210 AND K211 FLUIDOTHERAPY UNITS is an FDA 510(k)-cleared medical device (K871802) manufactured by Henley Intl.. 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 September 3, 1987. Regulation: 8.