ClearanceBrief
510(k) K953887 ยท IKT Electrode, Needle, Diagnostic Electromyograph

RE-USABLE CONCENTRIC NEEDLE

ApplicantChalgren Enterprises, Inc., Gilroy CA, US
DecisionSubstantially Equivalent, Oct 31, 1995
ReceivedAug 17, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953887

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.