ClearanceBrief
510(k) K841929 ยท FKX System, Peritoneal, Automatic Delivery

LIFEMED LIFECOIL CATHETERS

ApplicantLifemed of California, Walker MI, US
DecisionSubstantially Equivalent, Aug 8, 1984
ReceivedMay 10, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841929

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.