ClearanceBrief
510(k) K895460 ยท IKT Electrode, Needle, Diagnostic Electromyograph

CONCENTRIC ELECTRODE TYPE #13R01, 13R02

ApplicantDantec Electronics, Inc., Allendale NJ, US
DecisionSubstantially Equivalent, Jun 18, 1990
ReceivedSep 6, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895460

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.