510(k) K072237 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETOM VERIO
| Applicant | Siemens Medical Solutions USA, Inc., Mavern PA, US |
| Decision | Substantially Equivalent, Oct 10, 2007 |
| Received | Aug 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072237
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 30, 2025 | Siemens Medical Solutions USA, Inc MAGNETOM Verio. Model Number: 10276755. Open, Classified |
LNH | None listed |
| Sep 26, 2012 | Siemens Medical Solutions USA, Inc Siemens Magnetom Skyra, Verio, Spectra and Biograph MMR
Nuclear Magnetic Resonance Imaging System and Tomographic Imager Terminated |
LNH | None listed |
| Apr 2, 2012 | Siemens Medical Solutions USA, Inc Siemens MAGNETOM Verio
Use: Nuclear resonance imaging system Terminated |
LNH | None listed |
| Feb 23, 2011 | Siemens Medical Solutions USA, Inc MAGNETOM Verio
Nuclear magnetic resonance imaging Terminated |
LNH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.