510(k) K193324 ยท LNH System, Nuclear Magnetic Resonance Imaging
Motion Correction System
| Applicant | Kineticor, Inc., Honolulu HI, US |
| Decision | Substantially Equivalent, Feb 4, 2020 |
| Received | Dec 2, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193324
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.