WAVi SCAN EEG System and Accessories

WAVi SCAN EEG System and Accessories is an FDA 510(k)-cleared medical device (K213900) 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 May 5, 2022. Regulation: 8.