ClearanceBrief
510(k) K132617 ยท DYB Introducer, Catheter

MEDTRONIC INPUT PS INTRODUCER

ApplicantMedtronic, Inc., Danvers MA, US
DecisionSubstantially Equivalent, Apr 30, 2014
ReceivedAug 21, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132617

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.