510(k) K982339 ยท MOS Coil, Magnetic Resonance, Specialty
FLOW 7000 PERIPHERAL VASCULAR COIL
| Applicant | Usa Instruments, Inc., Aurora OH, US |
| Decision | Substantially Equivalent, Sep 4, 1998 |
| Received | Jul 6, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982339
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.