ClearanceBrief
510(k) K220506 ยท QAI Powered Microneedle Device

SkinPen Precision System

ApplicantCrown Aesthetics, Dallas TX, US
DecisionSubstantially Equivalent, Mar 7, 2022
ReceivedFeb 22, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K220506

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.