ClearanceBrief
510(k) K770790 ยท HCC Device, Biofeedback

FEEDBACK EDR SYSTEM MODEL EDR-100

ApplicantBio-Feedback Systems, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 10, 1977
ReceivedMay 2, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770790

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.