510(k) K980691 ยท MOS Coil, Magnetic Resonance, Specialty
AIRIS MAGNETIC RESONANCE DIAGNOSTIC DEVICE
| Applicant | Hitachi Medical Systems America, Inc., Twinsburg OH, US |
| Decision | Substantially Equivalent, May 11, 1998 |
| Received | Feb 23, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980691
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.