GSR, 126, EEG 130-TEMP. 132, EMG 133

GSR, 126, EEG 130-TEMP. 132, EMG 133 is an FDA 510(k)-cleared medical device (K841895) manufactured by Calnor of EL Paseo, 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 July 16, 1984. Regulation: 8.