510(k) K953918 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETIC RESONANCE DIAGNOSTIC DEVICE
| Applicant | Hitachi Medical Systems America, Inc., Twinsburg OH, US |
| Decision | Substantially Equivalent, Sep 12, 1995 |
| Received | Aug 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953918
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.