ClearanceBrief
510(k) K082467 ยท DQK Computer, Diagnostic, Programmable

ENSITE FUSION DYNAMIC REGISTRATION TOOL

ApplicantSt Jude Medical, St. Paul MN, US
DecisionSubstantially Equivalent, Sep 11, 2008
ReceivedAug 27, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082467

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.