510(k) K912095 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETIC RESONANCE DIAGNOSTIC DEVICE
| Applicant | Siemens Medical Solutions USA, Inc., Iselin NJ, US |
| Decision | Substantially Equivalent, Aug 9, 1991 |
| Received | May 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912095
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.