510(k) K232680 ยท LNH System, Nuclear Magnetic Resonance Imaging
fMRI Hardware System
| Applicant | Nordicneurolab AS, Bergen, NO |
| Decision | Substantially Equivalent, Dec 13, 2023 |
| Received | Sep 1, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232680
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.