ClearanceBrief
510(k) K915215 ยท LFK Catheter, Femoral

CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITS

ApplicantAkcess Medical Products, Inc., New Brunswick NJ, US
DecisionUnknown, Mar 27, 1992
ReceivedNov 18, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915215

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.