ClearanceBrief
510(k) K872250 ยท GXY Electrode, Cutaneous

LECTEC STIMULATING ELECTRODE

ApplicantLectec Corp., Minnetonka MN, US
DecisionSubstantially Equivalent, Aug 7, 1987
ReceivedJun 12, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K872250

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.