510(k) K232235 · OBP Transcranial Magnetic Stimulator
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., Whitland, GB |
| Decision | Substantially Equivalent, Oct 25, 2023 |
| Received | Jul 27, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232235
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.