ClearanceBrief
510(k) K230506 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

PureLift Pro Edition

ApplicantXtreem Pulse, New York NY, US
DecisionSubstantially Equivalent, Jun 21, 2023
ReceivedFeb 24, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K230506

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.