NEURO CHANNEL ENDOSCOPE MODEL 2232

NEURO CHANNEL ENDOSCOPE MODEL 2232 is an FDA 510(k)-cleared medical device (K945633) 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 September 18, 1995. Regulation: 8.