ClearanceBrief
510(k) K151497 ยท MMX Device, Percutaneous Retrieval

EN Snare Endovascular Snare System

ApplicantMerit Medical Systems, Inc., Galway, IE
DecisionSubstantially Equivalent, Jul 1, 2015
ReceivedJun 4, 2015
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K151497

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.