510(k) DEN180008 ยท QCR Wound Autofluorescence Imaging Device
MolecuLight i:X
| Applicant | MolecuLight, Inc., Toronto, CA |
| Decision | Unknown, Jul 31, 2018 |
| Received | Feb 16, 2018 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN180008
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.