FDA 510(k) Applications Submitted by GN RESOUND A/S
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150171 | 01/26/2015 | Tinnitus Sound Generator Module | GN RESOUND A/S |
| K110932 | 04/04/2011 | TINNITUS SOUND GENERATOR MODULE | GN RESOUND A/S |
| K073636 | 12/26/2007 | TINNITUS SOUND GENERATOR MODULE | GN RESOUND A/S |
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