ClearanceBrief
510(k) K842288 ยท HCC Device, Biofeedback

EEG 130

ApplicantCalnor of EL Paseo, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 17, 1984
ReceivedMay 7, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842288

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.