AESCULAP VENTRICULOSCOPE SYSTEM

AESCULAP VENTRICULOSCOPE SYSTEM is an FDA 510(k)-cleared medical device (K954394) manufactured by Aesculap, 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 March 6, 1996. Regulation: 8.