ClearanceBrief
510(k) K935853 ยท HCC Device, Biofeedback

EMG TRAINER

ApplicantUnitech, Madison WI, US
DecisionSubstantially Equivalent, Jan 18, 1995
ReceivedDec 8, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935853

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.