ClearanceBrief
510(k) K895580 ยท DYB Introducer, Catheter

Y-ADAPTER W/THOUY BORST

ApplicantAngeion Corp., Plymouth MN, US
DecisionSubstantially Equivalent, Apr 30, 1990
ReceivedSep 15, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895580

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.