Class Class II

Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+ (K222171)

K222171 2023-01-13 Traditional
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Description

Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+ by Magstim Company, Ltd. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222171
Clearance Date2023-01-13
Clearance TypeTraditional
Product CodeOBP
Regulation Number882.5805

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