Last synced on 7 June 2024 at 11:04 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232235
510(k) Type
Traditional
Applicant
The Magstim Company Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/25/2023
Days to Decision
90 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232235
510(k) Type
Traditional
Applicant
The Magstim Company Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/25/2023
Days to Decision
90 days
Submission Type
Summary