ClearanceBrief
510(k) K882062 ยท HCC Device, Biofeedback

MODEL BIOSTAR

ApplicantTargus Concepts, Redwood City CA, US
DecisionSubstantially Equivalent, Jun 17, 1988
ReceivedMay 16, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882062

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.