FDA 510(k) Applications Submitted by MEDOVENT GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180222 | 01/25/2018 | Reaxon Plus | Medovent GmbH |
| K143711 | 12/29/2014 | Reaxon Plus | MEDOVENT GMBH |
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