510(k) K993574 ยท LNH System, Nuclear Magnetic Resonance Imaging
OPART/PRODIGA, OPART/PROTENZA, OPART/PARAGON
| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Jan 18, 2000 |
| Received | Oct 21, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993574
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.