ClearanceBrief
510(k) K242977 ยท FTC Light, Ultraviolet, Dermatological

308nm Excimer Phototherapy Device (CN-308E, KN-4003B3, KN-4003B4, KN-5000C KN-5000D, KN-5000H, KN-5000K)

ApplicantXuzhou Kernel Medical Equipment Co., Ltd., Xuzhou, CN
DecisionSubstantially Equivalent, Feb 6, 2025
ReceivedSep 26, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242977

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.