510(k) K013595 ยท MOS Coil, Magnetic Resonance, Specialty
PREMIER III PHASED ARRAY CTL SPINE COIL
| Applicant | Usa Instruments, Inc., Aurora OH, US |
| Decision | Substantially Equivalent, Jan 22, 2002 |
| Received | Oct 30, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013595
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.