510(k) K242908 ยท FTC Light, Ultraviolet, Dermatological
UV Phototherapy Device (Group A: SQ308PCHFD, SQ308PCQFD, SQ308PCPFD, SQ308PCNFD, SQ308PCMFD); UV Phototherapy Device (Group B: SQ308PHTFF, SQ308PHSFF, SQ308PHRFF, SQ308PHZFG, SQ308PPUFF, SQ308PPVFF, SQ308PPWFG)
| Applicant | Shanghai Sigma High-Tech Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Dec 19, 2024 |
| Received | Sep 24, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242908
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.