510(k) K233564 · QDG Parathyroid Autofluorescence Imaging Device
FLUOBEAM® LX Imaging System (FB-LX); FLUOBEAM® LX Red Imaging System (FB-LXR)
| Applicant | Fluoptics Sas (A Getinge Group Company), Grenoble, FR |
| Decision | Substantially Equivalent, Dec 15, 2023 |
| Received | Nov 6, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233564
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.