AESCULAP ANGLED NEUROENDOSCOPES

AESCULAP ANGLED NEUROENDOSCOPES is an FDA 510(k)-cleared medical device (K964281) 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 April 20, 1997. Regulation: 8.