Remote Diagnostic Technologies , Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2018-01-10
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K173768 | Tempus Pro Patient Monitor | MHX | 2018-01-10 | View |
| 510(k) | K170567 | Tempus Pro Patient Monitor | MHX | 2017-07-06 | View |
No matching devices.