510(k) K183222 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETOM Terra
| Applicant | Siemens Medical Solutions USA, Inc., Malvern PA, US |
| Decision | Substantially Equivalent, Feb 15, 2019 |
| Received | Nov 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183222
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.