510(k) K910220 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETIC RESONANCE DEVICE ACCESSORY, SM PARTS COIL
| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Mar 25, 1991 |
| Received | Jan 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910220
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.