Last synced on 19 July 2024 at 11:05 pm

Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223154
510(k) Type
Traditional
Applicant
Magstim Company Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/16/2023
Days to Decision
161 days
Submission Type
Summary

Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223154
510(k) Type
Traditional
Applicant
Magstim Company Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/16/2023
Days to Decision
161 days
Submission Type
Summary