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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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