510(k) DEN170092 ยท QDG Parathyroid Autofluorescence Imaging Device
Fluobeam 800 Clinic Imaging Device used with Fluocase 800 Control System
| Applicant | Fluoptics, Grenoble Cedex 9, FR |
| Decision | Unknown, Nov 2, 2018 |
| Received | Dec 22, 2017 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN170092
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.