ClearanceBrief
510(k) K030277 ยท MSD Catheter, Hemodialysis, Implanted

SOFT-CELL DUAL LUMEN CATHETERS

ApplicantC.R. Bard, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Aug 6, 2003
ReceivedJan 27, 2003
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K030277

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.