CLARUS NEUROPEN MODEL 2120

CLARUS NEUROPEN MODEL 2120 is an FDA 510(k)-cleared medical device (K942249) manufactured by Clarus Medical Systems, 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 3, 1994. Regulation: 8.