510(k) K001210 ยท MOS Coil, Magnetic Resonance, Specialty
HI-RES 9000 PHASED ARRAY CAROTID COIL
| Applicant | Usa Instruments, Inc., Aurora OH, US |
| Decision | Substantially Equivalent, Jun 9, 2000 |
| Received | Apr 14, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001210
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.