ClearanceBrief
510(k) K192733 ยท IPF Stimulator, Muscle, Powered

RelieforMe TENS/EMS Device Model UPK-GE01

ApplicantUmeheal , Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Dec 23, 2019
ReceivedSep 27, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192733

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.