ClearanceBrief
510(k) K911236 ยท DYB Introducer, Catheter

MEDTRONIC PERMANENT LEAD INTRODUCER, VARIOUS MDLS

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Jun 18, 1991
ReceivedMar 20, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911236

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.