510(k) K010730 ยท MOS Coil, Magnetic Resonance, Specialty
MODIFICATION TO FLOW 7000 PERIPHERAL VASCULAR COIL
| Applicant | Usa Instruments, Inc., Aurora OH, US |
| Decision | Substantially Equivalent, May 16, 2001 |
| Received | Mar 12, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010730
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.