ClearanceBrief
510(k) K022238 ยท DWS Instruments, Surgical, Cardiovascular

MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Oct 9, 2002
ReceivedJul 11, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K022238

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.