FDA 510(k) Applications Submitted by Daniel Gregory

FDA 510(k) Number	Submission Date	Device Name	Applicant
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
K232235	07/27/2023	Magstim«Horizon« 3.0 TMS Therapy System; Horizon« 3.0 System; Horizon« 3.0; Horizon« 3.0 with Navigation; Horizon« 3.0 with StimGuide Pro	The Magstim Company Ltd.