510(k) K132951 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETOM AERA
| Applicant | Siemens Medical Solutions USA, Inc., Mavern PA, US |
| Decision | Substantially Equivalent, Nov 15, 2013 |
| Received | Sep 19, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132951
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 22, 2015 | Siemens Medical Solutions USA, Inc MAGNETOM systems, magnetic resonance diagnostic devices (MRDD). Terminated |
LNH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.