510(k) K920835 ยท LNH System, Nuclear Magnetic Resonance Imaging
PRESATURATION
| Applicant | Resonex, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, May 22, 1992 |
| Received | Feb 24, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920835
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.