ClearanceBrief
510(k) K880980 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

SCHULDT* PC* - DUAL CHANNEL TENS

ApplicantSchuldt Laboratories, Inc., Canada, CA
DecisionSubstantially Equivalent, Apr 11, 1988
ReceivedMar 8, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880980

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.