FDA 510(k) Applications Submitted by MAGSTIM COMPANY LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K162935 10/20/2016 Rapid2 Therapy System MAGSTIM COMPANY LTD.
K203684 12/17/2020 Neurosign V4 Intraoperative Nerve Monitor Magstim Company Ltd.
K180907 04/06/2018 HORIZON TMS Therapy System Magstim Company Ltd.
K171051 04/10/2017 HORIZON Therapy System Magstim Company Ltd.
K211389 05/05/2021 Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, Horizon 3.0 with Navigation Magstim Company Ltd.
K181559 06/13/2018 Neurosign V4 Intraoperative Nerve Monitor Magstim Company Ltd.
K223154 10/06/2022 Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+ Magstim Company Ltd.
K182853 10/10/2018 HORIZON TMS Therapy System Magstim Company Ltd.
K183376 12/06/2018 HORIZON TMS Therapy System with Navigation Magstim Company Ltd.


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