ClearanceBrief
510(k) K913801 ยท DYB Introducer, Catheter

CORDIS CATH SHEATH INTRO SYST PLUS W/UNISTASIS VAL

ApplicantCordis Corp., Miami Lakes FL, US
DecisionSubstantially Equivalent, Oct 16, 1991
ReceivedAug 26, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913801

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.