ClearanceBrief
510(k) K900515 ยท DYB Introducer, Catheter

MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S)

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 23, 1990
ReceivedFeb 2, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900515

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.