510(k) K190891 ยท QDG Parathyroid Autofluorescence Imaging Device
Fluobeam LX
| Applicant | Fluoptics, Grenoble Cedex 9, FR |
| Decision | Substantially Equivalent, Jul 31, 2019 |
| Received | Apr 5, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190891
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.