510(k) K173436 ยท FTC Light, Ultraviolet, Dermatological
Luma Light System
| Applicant | Luma Therapeutics, Millbrae CA, US |
| Decision | Substantially Equivalent, Jan 30, 2018 |
| Received | Nov 3, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173436
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.