ClearanceBrief
510(k) K841718 ยท

FREKATHETER VENOUS CATHETERISATION SYS

ApplicantFresenius USA, Inc., Walker MI, US
DecisionUnknown, Apr 25, 1984
ReceivedApr 25, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841718

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.