Magstim Company, Ltd.
Magstim Company, Ltd. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2023.
Top product codes for Magstim Company, Ltd.
Recent clearances by Magstim Company, Ltd.
- K223154 — Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+
- K222171 — Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+
- K211389 — Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, Horizon 3.0 with Navigation
- K203684 — Neurosign V4 Intraoperative Nerve Monitor
- K183376 — HORIZON TMS Therapy System with Navigation
- K182853 — HORIZON TMS Therapy System
- K181559 — Neurosign V4 Intraoperative Nerve Monitor
- K180907 — HORIZON TMS Therapy System
- K171051 — HORIZON Therapy System
- K162935 — Rapid2 Therapy System
Data sourced from openFDA. This site is unofficial and independent of the FDA.