Vios Medical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2018-07-26
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K173107 | Vios Central Station Monitor Software, Vios Central Server Software | DXJ | 2018-07-26 | View |
| 510(k) | K172586 | Vios Monitoring System™ Model 2050 | DRT | 2018-06-22 | View |
No matching devices.