Akesis, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2021-03-05
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K203146 | Akesis Galaxy RTi | IWB | 2021-03-05 | View |
| 510(k) | K200050 | Akesis Galaxy RTx | IWB | 2020-02-04 | View |
| 510(k) | K190844 | Akesis Galaxy | IWB | 2019-09-04 | View |
No matching devices.