ClearanceBrief
510(k) K220503 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

TENS device-EmeTerm 2, Model: YF-ZTY-E2

ApplicantWat Medical Technology, Inc., Ningbo, CN
DecisionSubstantially Equivalent, Apr 23, 2022
ReceivedFeb 22, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220503

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.