ClearanceBrief
510(k) K821523 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

OMNI TENS

ApplicantOmni Intl., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 16, 1982
ReceivedMay 21, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821523

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.