Hi-Dow PRO TOUCH WIRELESS 6-12 (HD-19A)

Hi-Dow PRO TOUCH WIRELESS 6-12 (HD-19A) is an FDA 510(k)-cleared medical device (K233461) manufactured by Hi-Dow International, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 18, 2024. Regulation: 8.