510(k) K232322 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETOM Terra; MAGNETOM Terra.X
| Applicant | Siemens Medical Solutions USA, Inc., Malvern PA, US |
| Decision | Substantially Equivalent, Mar 22, 2024 |
| Received | Aug 3, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232322
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.