ClearanceBrief
510(k) K895506 ยท LFJ Catheter, Subclavian

FLEXXICON PLUS DUAL LUMEN DIALYSIS CATHETER

ApplicantVas-Cath, Inc., Mississauga, Ontario, CA
DecisionSubstantially Equivalent, Feb 9, 1990
ReceivedSep 12, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895506

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.