ClearanceBrief
510(k) K932430 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER

ApplicantPharmacia Deltec, Inc., St. Paul MN, US
DecisionUnknown, May 2, 1994
ReceivedMay 20, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932430

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.