ClearanceBrief
510(k) K071818 ยท DQK Computer, Diagnostic, Programmable

ENSITE FUSION DYNAMIC REGISTRATION TOOL

ApplicantSt Jude Medical, St. Paul MN, US
DecisionSubstantially Equivalent, Dec 20, 2007
ReceivedJul 3, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071818

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.