ClearanceBrief
510(k) K011015 ยท NFK Kit, Repair, Catheter, Hemodialysis

CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000

ApplicantC.R. Bard, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Jun 22, 2001
ReceivedApr 4, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K011015

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.