510(k) K173540 ยท OBP Transcranial Magnetic Stimulator
Brainsway Deep (DTMS) System
| Applicant | Brainsway , Ltd., Jerusalem, IL |
| Decision | Substantially Equivalent, May 3, 2018 |
| Received | Nov 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173540
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.