AMBULATORY EEG/SLEEP RECORDER AND ACCESSORIES, MODEL # SSR3201

AMBULATORY EEG/SLEEP RECORDER AND ACCESSORIES, MODEL # SSR3201 is an FDA 510(k)-cleared medical device (K983072) manufactured by Nihon Kohden America, 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 November 30, 1998. Regulation: 8.