
Carefusion 209, Inc.
Free shipping on orders over $99 · 30-day returns
NICOLET WIRELESS EEG is an FDA 510(k)-cleared medical device (K103140) manufactured by Carefusion 209, 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 April 7, 2011. Regulation: 8.