ACKERMANN EUROPCLIP

ACKERMANN EUROPCLIP is an FDA 510(k)-cleared medical device (K111930) manufactured by Ackermann Instrumente GmbH. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 7, 2011. Regulation: 8.