ClearanceBrief
510(k) K830877 ยท GYA Tester, Electrode/Lead, Electroencephalograph

AP-CHECK

ApplicantGeneral Devices, Mchenry IL, US
DecisionSubstantially Equivalent, Jun 8, 1983
ReceivedMar 18, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830877

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.