ClearanceBrief
510(k) K852446 ยท DTB Permanent Pacemaker Electrode

ENDOCARDIAL SCREW-IN LEAD WITH PLATINUM POROUS TIP

ApplicantDiag Corp., Minnetonka MN, US
DecisionSubstantially Equivalent, Sep 17, 1985
ReceivedJun 10, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852446

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.