ClearanceBrief
510(k) K961809 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

SHE-LI TENS STIMULATOR MODEL SL-101 RX

ApplicantMedi Consultants, Inc., Paterson NJ, US
DecisionSubstantially Equivalent, Feb 26, 1997
ReceivedMay 10, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961809

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.