ClearanceBrief
510(k) K834383 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT

ApplicantBurron Medical Products, Inc., Walker MI, US
DecisionSubstantially Equivalent, May 1, 1984
ReceivedDec 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834383

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.