ClearanceBrief
510(k) K081311 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

POWERPORT IMPLANTED PORT WITH GROSHONG CATHETER

ApplicantC.R. Bard, Inc., Salt Lake Ciy, UT, US
DecisionSubstantially Equivalent, Jun 4, 2008
ReceivedMay 9, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081311

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.