ClearanceBrief
510(k) K923935 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

SD-605 SD II PROGRAM

ApplicantSkylark Device Co., Ltd., Taipei, Taiwan, R.O.C., TW
DecisionSubstantially Equivalent, Oct 15, 1992
ReceivedAug 5, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923935

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.