510(k) K232361 ยท LNH System, Nuclear Magnetic Resonance Imaging
Promaxo MRI System II
| Applicant | Promaxo, Inc., Oakland CA, US |
| Decision | Substantially Equivalent, Sep 5, 2023 |
| Received | Aug 7, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232361
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.