ClearanceBrief
510(k) K914162 ยท LFJ Catheter, Subclavian

VAS-CATH FLEXXICON 2 DUAL LUMEN DIALYSIS CATHETERS

ApplicantVas-Cath, Inc., Mississauga,Ontario, CA
DecisionSubstantially Equivalent, Jul 1, 1993
ReceivedSep 17, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914162

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.