ClearanceBrief
510(k) K860570 ยท KRA Catheter, Continuous Flush

ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE

ApplicantParke-Davis Co., Rochester MI, US
DecisionSubstantially Equivalent, Mar 31, 1986
ReceivedFeb 14, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860570

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.