ClearanceBrief
510(k) K192296 ยท DQY Catheter, Percutaneous

Medtronic 6F Taiga Guiding Catheter

ApplicantMedtronic Vascular, Danvers MA, US
DecisionSubstantially Equivalent, Sep 20, 2019
ReceivedAug 23, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K192296

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.