Last synced on 21 June 2024 at 11:04 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
K222171
510(k) Type
Traditional
Applicant
Magstim Company Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/13/2023
Days to Decision
176 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
K222171
510(k) Type
Traditional
Applicant
Magstim Company Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/13/2023
Days to Decision
176 days
Submission Type
Summary