510(k) K913475 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETIC RESONANCE DIAGNOSTIC DEVICE
| Applicant | GE Medical Systems, Milwaukee WI, US |
| Decision | Substantially Equivalent, Oct 30, 1991 |
| Received | Aug 5, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913475
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.