510(k) K002179 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETOM ALLEGRA SYSTEM
| Applicant | Siemens Medical Solutions USA, Inc., Iselin NJ, US |
| Decision | Substantially Equivalent, Oct 11, 2000 |
| Received | Jul 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002179
| 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 |
| Feb 10, 2004 | Siemens Medical Solutions USA, Inc Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device Terminated |
None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.