510(k) K921720 ยท LNH System, Nuclear Magnetic Resonance Imaging
MRT-50A QD SPINE COIL
| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Jul 16, 1992 |
| Received | Apr 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921720
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.