EEG & RESPIRATION MODULES POLYGRAPH

EEG & RESPIRATION MODULES POLYGRAPH is an FDA 510(k)-cleared medical device (K823563) manufactured by Nihon Kohden America, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 11, 1983. Regulation: 8.