ClearanceBrief
510(k) K833354 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

AUTO-TENS MODEL VI DUAL CHANNEL BATT

ApplicantPhysio Tronics Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 28, 1983
ReceivedSep 28, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833354

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.