510(k) K926171 ยท LNH System, Nuclear Magnetic Resonance Imaging
MRT-150A, QD SPINE COIL
| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Apr 27, 1993 |
| Received | Dec 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926171
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.