ClearanceBrief
510(k) K842021 ยท HCC Device, Biofeedback

EEG BIOFEEDBACK DEVICE ACCESSORY

ApplicantElectronics Research & Production, Mchenry IL, US
DecisionSubstantially Equivalent, Jul 20, 1984
ReceivedMay 18, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842021

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.