ClearanceBrief
510(k) K201680 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

NuFACE Mini Plus

ApplicantCarole Cole Company, Vista CA, US
DecisionSubstantially Equivalent, Feb 19, 2021
ReceivedJun 22, 2020
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K201680

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.