510(k) K191032 ยท LNH System, Nuclear Magnetic Resonance Imaging
fMRI Hardware System
| Applicant | Nordicneurolab AS, Bergen, NO |
| Decision | Substantially Equivalent, Nov 27, 2019 |
| Received | Apr 18, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191032
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.