NICOLET PORATBLE SPIRIT SYSTEM

NICOLET PORATBLE SPIRIT SYSTEM is an FDA 510(k)-cleared medical device (K915652) manufactured by Nicolet Instrument Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 6, 1992. Regulation: 8.