ClearanceBrief
510(k) K162097 ยท DYB Introducer, Catheter

InTRAkit

ApplicantMedtronic Vascular, Danvers MA, US
DecisionSubstantially Equivalent, Nov 17, 2016
ReceivedJul 29, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K162097

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.