510(k) K222832 ยท NEU Marker, Radiographic, Implantable
Sentimag System
| Applicant | Endomagnetics Ltd.,, Cambridge, GB |
| Decision | Substantially Equivalent, Jan 21, 2023 |
| Received | Sep 20, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222832
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.