510(k) K911276 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETIC RESONANCE DEVICE ACCESSORY
| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Jun 28, 1991 |
| Received | Mar 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911276
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.