510(k) K250455 ยท QDG Parathyroid Autofluorescence Imaging Device
FLUOBEAM LX Imaging System (FBLX); FLUOBEAM LM Imaging System (FBLM)
| Applicant | Fluoptics Sas (A Getinge Group Company}, Grenoble, FR |
| Decision | Substantially Equivalent, Apr 17, 2025 |
| Received | Feb 18, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250455
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.