AESCULAP NEUROENDOSCOPE

AESCULAP NEUROENDOSCOPE is an FDA 510(k)-cleared medical device (K941239) 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 July 10, 1994. Regulation: 8.