AESCULAP NEURO PATTIES

AESCULAP NEURO PATTIES is an FDA 510(k)-cleared medical device (K062406) 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 September 14, 2006. Regulation: 8.