TENS PRO 900

TENS PRO 900 is an FDA 510(k)-cleared medical device (K915663) manufactured by Acuhealth (Usa) Pty. , 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 April 14, 1993. Regulation: 8.