TELEFACTOR D/EEG-32

TELEFACTOR D/EEG-32 is an FDA 510(k)-cleared medical device (K925838) manufactured by Grass-Telefactor Product Group. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 29, 1993. Regulation: 8.