ClearanceBrief
510(k) K241400 ยท QAI Powered Microneedle Device

SkinPen Precision Elite System

ApplicantCrown Aesthetics, Dallas TX, US
DecisionSubstantially Equivalent, Aug 29, 2024
ReceivedMay 17, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241400

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.