510(k) K180663 ยท KPR System, X-Ray, Stationary
LaVid FMTS DIAGNOSTIC X-RAY SYSTEM
| Applicant | Livermoretech, Inc., Plano TX, US |
| Decision | Substantially Equivalent, May 18, 2018 |
| Received | Mar 14, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180663
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.