ClearanceBrief
510(k) K031718 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

LIFEVALVE CENTRAL VENOUS CATHTER

ApplicantHorizon Medical Products, Inc., Manchester GA, US
DecisionSubstantially Equivalent, Jul 2, 2003
ReceivedJun 3, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K031718

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.