FDA 510(k) Applications Submitted by HASOMED GmbH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K162683 | 09/26/2016 | RehaStim 2 | HASOMED GmbH |
| K132416 | 08/02/2013 | REHASTIM 2, ERIGOPRO (FES) | HASOMED GMBH |
| K112844 | 09/29/2011 | REHASTIM 2, REHAMOVE 2 | HASOMED GMBH |
| K073237 | 11/16/2007 | REHASTIM & REHAMOVE | HASOMED GMBH |
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