ClearanceBrief
510(k) K843642 ยท DYB Introducer, Catheter

SUBCLAVIAN LEAD INTRODUCER SYS

ApplicantXanmed Corp., Walker MI, US
DecisionSubstantially Equivalent, Oct 23, 1984
ReceivedSep 17, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843642

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.