K232235

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

510(k) number: K232235
Device name: 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
Applicant: The Magstim Company , Ltd. GB
Product code: OBP — Transcranial Magnetic Stimulator
Decision date: 2023-10-25
Date received: 2023-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Advisory committee: Neurology

Also available from FDA: K232235.pdf

Official FDA record: K232235

Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.