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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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