EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908

EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908 is an FDA 510(k)-cleared medical device (K110509) manufactured by Everyway Medical Instruments Co.,Ltd. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 19, 2011. Regulation: 8.