CLARUS PHOENIX NEURO ENDOSCOPE MODEL 2160

CLARUS PHOENIX NEURO ENDOSCOPE MODEL 2160 is an FDA 510(k)-cleared medical device (K945296) 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 July 13, 1995. Regulation: 8.