ClearanceBrief
510(k) K080304 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

PRO TENS, MODEL WL-240 RX

ApplicantWell-Life Healthcare Limited, Yunghe City, Taipei County, TW
DecisionSubstantially Equivalent, Jun 20, 2008
ReceivedFeb 5, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K080304

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.