Fifth Eye, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest Approval2022-07-14
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K221203 | AHI System | QNV | 2022-07-14 | View |
| 510(k) | K212219 | AHI System | QNV | 2021-12-03 | View |
| 510(k) | DEN200022 | Analytic for Hemodynamic Instability (AHI) | QNV | 2021-03-01 | View |
No matching devices.