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Electrical Geodesics, Incorporated
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GEODESIC EEG SYSTEM, MODEL 200 is an FDA 510(k)-cleared medical device (K012079) manufactured by Electrical Geodesics, Incorporated. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 18, 2001. Regulation: 8.