510(k) DEN230008 ยท QZS Software-Aided Adjunctive Diagnostic Device For Use By Physicians On Lesions Suspicious For Skin Cancer
DermaSensor
| Applicant | Dermasensor, Inc., Miami FL, US |
| Decision | Unknown, Jan 12, 2024 |
| Received | Feb 2, 2023 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN230008
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.