ClearanceBrief
510(k) K182424 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

NuFACE FIX Skin Toning Device

ApplicantCarol Cole Company Dba Nuface, Vista CA, US
DecisionSubstantially Equivalent, Dec 18, 2018
ReceivedSep 6, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182424

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.