WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts

WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts is an FDA 510(k)-cleared medical device (K162460) manufactured by Wavi Co.. 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 27, 2017. Regulation: 8.