CEEGRAPH TRAVELER AMBULATORY EEG RECORDER

CEEGRAPH TRAVELER AMBULATORY EEG RECORDER is an FDA 510(k)-cleared medical device (K954954) manufactured by Bio-Logic Systems Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 24, 1996. Regulation: 8.