510(k) K983110 ยท LNH System, Nuclear Magnetic Resonance Imaging
FLEXART,FLEXART/HYPER, VISART, VISART/HYPER
| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Feb 25, 1999 |
| Received | Sep 4, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983110
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.