ClearanceBrief
510(k) K230782 ยท PCC Stimulator, Nerve, Electrical, Transcutaneous, For Migraine

TENS device-HeadaTerm 2 (Model: YF-HT2)

ApplicantWat Medical Technology, Inc., Ningbo, CN
DecisionSubstantially Equivalent, Feb 26, 2024
ReceivedMar 22, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230782

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.