ClearanceBrief
510(k) K072278 ยท DRC Trocar

BRK TRANSSEPTAL NEEDLE

ApplicantSt Jude Medical, Minnetonka MN, US
DecisionSubstantially Equivalent, Sep 13, 2007
ReceivedAug 16, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072278

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.