FDA 510(k) Applications Submitted by The Magstim Company Limited

FDA 510(k) Number	Submission Date	Device Name	Applicant
K243869	12/17/2024	Horizon« 3.0 TMS Therapy System (Horizon 3.0 Inspire); Horizon« 3.0 TMS Therapy System (Horizon 3.0 with StimGuide Pro); Horizon« 3.0 TMS Therapy System (Horizon 3.0)	The Magstim Company Limited
K250286	01/31/2025	Rapid2 Magnetic Stimulators (Magstim Rapid2, Magstim Super Rapid2, Magstim Super Rapid2 Plus1)	The Magstim Company Limited
K241518	05/29/2024	Horizon« 3.0 TMS Therapy System (Horizon 3.0 Inspire); Horizon« 3.0 TMS Therapy System (Horizon 3.0 with StimGuide Pro); Horizon« 3.0 TMS Therapy System (Horizon 3.0)	The Magstim Company Limited