EE1114, 1118, 1121 ELECTRO-ENCEPHALOGRAPH

EE1114, 1118, 1121 ELECTRO-ENCEPHALOGRAPH is an FDA 510(k)-cleared medical device (K903004) manufactured by Teca, 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 November 14, 1990. Regulation: 8.