ClearanceBrief
510(k) K812173 ยท KRA Catheter, Continuous Flush

FLUSHFLO II

ApplicantBentley Laboratories, Inc., Walker MI, US
DecisionSubstantially Equivalent, Aug 18, 1981
ReceivedAug 3, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812173

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.