ClearanceBrief
510(k) K872399 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

T.E.N.S. DEVICE MODEL SPL 2000S

ApplicantSpartan Laboratories, Inc., Las Vegas NV, US
DecisionSubstantially Equivalent, Jul 27, 1987
ReceivedJun 22, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K872399

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.