ClearanceBrief
510(k) K830876 ยท KRC Tester, Electrode, Surface, Electrocardiographic

PREP-CHECK

ApplicantGeneral Devices, Bergenfield NJ, US
DecisionSubstantially Equivalent, May 18, 1983
ReceivedMar 18, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830876

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.