510(k) K250425 ยท FTC Light, Ultraviolet, Dermatological
Ultraviolet Phototherapy Device
| Applicant | APK Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Apr 7, 2025 |
| Received | Feb 14, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250425
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.