FDA 510(k) Applications Submitted by THE MAGSTIM COMPANY LTD.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K051864	07/08/2005	MAGSTIM RAPID2, MAGSTIM SUPER RAPID2, MODELS 3004-000, 3005-00	THE MAGSTIM COMPANY LTD.
K080499	02/25/2008	MAGSTIM DOUBLE 70MM AIR FILM COIL, MODEL 3910-00	THE MAGSTIM COMPANY LTD.
K071349	05/14/2007	NEUROSIGN LARYNGEAL ELECTRODES	THE MAGSTIM COMPANY LTD.
K083242	11/03/2008	NEUROSIGN AVALANCHE MOTOR NERVE MONITOR	THE MAGSTIM COMPANY LTD.
K964869	12/04/1996	NEUROSIGN 800, 8 CHANNEL MOTOR NERVE MONITOR	THE MAGSTIM COMPANY LTD.
K980148	01/15/1998	NEUROSIGN 800, 8 CHANNEL MOTOR NERVE MONITOR	THE MAGSTIM COMPANY LTD.
K053141	11/09/2005	NEUROSIGN MOTOR NERVE MONITOR, MODELS NEUROSIGN 400 & 800	THE MAGSTIM COMPANY LTD.
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.
K130403	02/19/2013	MAGSTIM DOUBLE 70-2 COIL	THE MAGSTIM COMPANY LTD.
K991583	05/07/1999	NEUROSIGN 400, 4 CHANNEL MOTOR NERVE MONITOR	THE MAGSTIM COMPANY LTD.