ClearanceBrief
510(k) K941938 ยท HCC Device, Biofeedback

THE MIRAGE SYSTEM BIOFEEDBACK INTERFACE

ApplicantIntercare Diagnostics, Inc., Inglewood CA, US
DecisionSubstantially Equivalent, Aug 5, 1994
ReceivedApr 21, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K941938

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.