510(k) K230076 · FTC Light, Ultraviolet, Dermatological
Enhanced AURORA Medical Diode System, and related accessories
| Applicant | Psoria-Shield, Inc., Utica NY, US |
| Decision | Substantially Equivalent, Mar 8, 2023 |
| Received | Jan 10, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230076
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.