510(k) K031366 ยท MOS Coil, Magnetic Resonance, Specialty
PREMIER 9000 8 CHANNEL PHASED ARRAY CTL SPINE COIL
| Applicant | Usa Instruments, Inc., Aurora OH, US |
| Decision | Substantially Equivalent, Jul 11, 2003 |
| Received | Apr 30, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031366
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.