510(k) K945665 ยท LNH System, Nuclear Magnetic Resonance Imaging
FLEXART(TM) QD C-SPINE COIL
| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Apr 6, 1995 |
| Received | Nov 17, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945665
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.