ClearanceBrief
510(k) K891992 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

TENZCARE STIMULATOR 6890

Applicant3M Company, Cottae Grove MN, US
DecisionSubstantially Equivalent, Oct 12, 1989
ReceivedMar 28, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K891992

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.