Canadian Pioneer Medical Technology Corporation
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2022-02-25
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K211722 | Laser treatment system , models Nyx plus, Grace plus, Nemesis, Ares | GEX | 2022-02-25 | View |
| 510(k) | K212793 | Laser Treatment System, Model: Hera, Armo | GEX | 2021-10-25 | View |
| 510(k) | K210033 | Laser Treatment System, Model: NYX and Grace | GEX | 2021-02-26 | View |
No matching devices.