510(k) K920199 ยท LNH System, Nuclear Magnetic Resonance Imaging
HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST
| Applicant | Philips Medical Systems (Cleveland), Inc., Highland Heights OH, US |
| Decision | Substantially Equivalent, Mar 6, 1992 |
| Received | Jan 15, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920199
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.