ClearanceBrief
510(k) K230420 ยท QAI Powered Microneedle Device

Dr. pen Microneedling System

ApplicantGuangzhou Ekai Electronic Technology Co., Ltd., Guangzhou, CN
DecisionSubstantially Equivalent, Aug 11, 2023
ReceivedFeb 16, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230420

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.