510(k) K240571 ยท LNH System, Nuclear Magnetic Resonance Imaging
OASIS MRI System
| Applicant | Fujifilm Healthcare Corporation, Kashiwa-Shi, JP |
| Decision | Substantially Equivalent, Apr 12, 2024 |
| Received | Feb 29, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240571
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.