ClearanceBrief
510(k) K924010 ยท FPA Set, Administration, Intravascular

REDINOV PERFUSION SET

ApplicantBipress, Inc., Miami FL, US
DecisionSubstantially Equivalent, Aug 15, 1994
ReceivedAug 10, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924010

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.