FDA 510(k) Applications Submitted by Magstim Company Ltd
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222171 | 07/21/2022 | Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+ | Magstim Company Ltd |
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