ClearanceBrief
510(k) K011964 ยท HCC Device, Biofeedback

INSIGHT MILLENNIUM PLUS

ApplicantFasstech, Burlington MA, US
DecisionSubstantially Equivalent, Sep 20, 2001
ReceivedJun 25, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K011964

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.