510(k) K914114 ยท LNH System, Nuclear Magnetic Resonance Imaging
2DTOF MAGNETIC RESONANCE ANGIOGRAPH (MRA)
| Applicant | Resonex, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Dec 4, 1991 |
| Received | Sep 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914114
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.