ClearanceBrief
510(k) K821004 ยท DYG Catheter, Flow Directed

MEDTRONIC S3 TM SYSTEM

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, May 25, 1982
ReceivedApr 9, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821004

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.