Wavi Co.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2022-05-06
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213900 | WAVi SCAN EEG System and Accessories | GWQ | 2022-05-06 | View |
| 510(k) | K162460 | WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts | GXY | 2017-04-28 | View |
No matching devices.