510(k) K944662 ยท LNH System, Nuclear Magnetic Resonance Imaging
FLEXART QD BODY COIL
| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Jan 25, 1995 |
| Received | Sep 21, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944662
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.