FDA 510(k) Applications Submitted by ergoline GmbH

FDA 510(k) Number Submission Date Device Name Applicant
K212883 09/10/2021 ers2 - ergoline Rehabilitation System ergoline GmbH
K112121 07/25/2011 ERGOSELECT/GE ERGOLINE GMBH
K053078 11/02/2005 ERGOSELECT 100 K/P, ERGOSELECT 200 K/P ERGOLINE GMBH


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