ELAN 4 Electro Motor System Tools

ELAN 4 Electro Motor System Tools is an FDA 510(k)-cleared medical device (K172709) 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 October 16, 2018. Regulation: 8.