
Cyberkinetics, Inc. (Cki)
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NEUROPORT RECORDING MICROELECTRODE ARRAY SYSTEM is an FDA 510(k)-cleared medical device (K042384) manufactured by Cyberkinetics, Inc. (Cki). This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 28, 2005. Regulation: 8.