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Neurovirtual USA, Inc.
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BWIII EEG, BWIII EEG PLUS, BWIII PSG, BWIII PSG PLUS is an FDA 510(k)-cleared medical device (K112107) manufactured by Neurovirtual USA, 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 October 27, 2011. Regulation: 8.