ClearanceBrief
510(k) K222568 · OBJ Catheter, Ultrasound, Intravascular

OptiCross™ 18 Peripheral Imaging Catheter

ApplicantBoston Scientific Corporation, Maple Grove MN, US
DecisionSubstantially Equivalent, Sep 23, 2022
ReceivedAug 24, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K222568

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.