ClearanceBrief
510(k) K030442 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, Jul 21, 2003
ReceivedFeb 11, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030442

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.