FDA 510(k) Applications Submitted by NEUROTHERAPIES RESET GMBH.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K151558 | 06/10/2015 | Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro System | NEUROTHERAPIES RESET GMBH. |
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