Sinusys Corporation
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K160770 | Vent-Os Sinus Dilation family | LRC | 2016-06-29 | View |
| 510(k) | K133016 | VENT-OS SINUS DILATION SYSTEM | LRC | 2013-12-09 | View |
No matching devices.
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