ClearanceBrief
510(k) K895044 ยท DYB Introducer, Catheter

DUAL GUIDE INTRODUCER CATHETER

ApplicantCook, Inc., Bloomington IN, US
DecisionSubstantially Equivalent, Feb 26, 1990
ReceivedAug 9, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895044

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.