DizzyDoctor System 1.0.0

DizzyDoctor System 1.0.0 is an FDA 510(k)-cleared medical device (K182214) manufactured by Dizzydoctor Systems, LLC. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 13, 2018. Regulation: 8.