510(k) K915567 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY)
| Applicant | Fonar Corp., Melville NY, US |
| Decision | Substantially Equivalent, May 15, 1992 |
| Received | Dec 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915567
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.