510(k) K171051 ยท OBP Transcranial Magnetic Stimulator
HORIZON Therapy System
| Applicant | Magstim Company, Ltd., Whitland, GB |
| Decision | Substantially Equivalent, Sep 13, 2017 |
| Received | Apr 10, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171051
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.