ClearanceBrief
510(k) K844433 ยท LFJ Catheter, Subclavian

VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA

ApplicantVas-Cath of Canada , Ltd., Ontario, L5a 3v3, CA
DecisionSubstantially Equivalent, Mar 13, 1985
ReceivedNov 16, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844433

DateFirm and productCodeLinked 510(k)
Sep 20, 2007C.R. Bard Access Systems, Inc
Guidewire, 70cm x 1mm, REF 5583705, Sterile, Single Use, BARD Access Systems, Hemodialysis Catheter, Salt Lake City, UT 84116.
Terminated
MPBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.