ClearanceBrief
510(k) K190581 ยท DQY Catheter, Percutaneous

Amplatzer Trevisio Intravascular Delivery System

ApplicantABBOTT MEDICAL, Plymouth MN, US
DecisionSubstantially Equivalent, Apr 5, 2019
ReceivedMar 6, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K190581

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.