DISPOSIBLE EEG NEEDLE ELECTRODES

DISPOSIBLE EEG NEEDLE ELECTRODES is an FDA 510(k)-cleared medical device (K901280) manufactured by Medicotest, 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 May 10, 1990. Regulation: 8.