Magstim Company, Ltd.
FDA 510(k) & PMA Approved Devices — 10 products
Total Devices10
Categories2
Latest Approval2023-03-16
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K223154 | Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+ | OBP | 2023-03-16 | View |
| 510(k) | K222171 | Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+ | OBP | 2023-01-13 | View |
| 510(k) | K211389 | Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, Horizon 3.0 with Navigation | OBP | 2021-09-14 | View |
| 510(k) | K203684 | Neurosign V4 Intraoperative Nerve Monitor | PDQ | 2021-03-17 | View |
| 510(k) | K183376 | HORIZON TMS Therapy System with Navigation | OBP | 2019-04-03 | View |
| 510(k) | K182853 | HORIZON TMS Therapy System | OBP | 2019-03-15 | View |
| 510(k) | K181559 | Neurosign V4 Intraoperative Nerve Monitor | PDQ | 2018-11-09 | View |
| 510(k) | K180907 | HORIZON TMS Therapy System | OBP | 2018-08-03 | View |
| 510(k) | K171051 | HORIZON Therapy System | OBP | 2017-09-13 | View |
| 510(k) | K162935 | Rapid2 Therapy System | OBP | 2017-03-10 | View |
No matching devices.