EQUINOX DIGITAL EEG SYSTEM

EQUINOX DIGITAL EEG SYSTEM is an FDA 510(k)-cleared medical device (K962447) manufactured by Physiometrix, 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 December 11, 1996. Regulation: 8.