FDA 510(k) Applications Submitted by SINUSYS CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160770 | 03/21/2016 | Vent-Os Sinus Dilation family | SINUSYS CORPORATION |
| K133016 | 09/25/2013 | VENT-OS SINUS DILATION SYSTEM | SINUSYS CORPORATION |
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