ClearanceBrief
510(k) K202243 ยท QAI Powered Microneedle Device

SkinPen Precision System

ApplicantCrown Aesthetics, Dallas TX, US
DecisionSubstantially Equivalent, Apr 2, 2021
ReceivedAug 10, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K202243

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.