510(k) K230898 · QDG Parathyroid Autofluorescence Imaging Device
FLUOBEAM® LX Red
| Applicant | Fluoptics Sas, Grenoble, FR |
| Decision | Substantially Equivalent, Jul 28, 2023 |
| Received | Mar 31, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230898
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.