ClearanceBrief
510(k) K152157 ยท KRD Device, Vascular, For Promoting Embolization

LC Bead LUMI

ApplicantBiocompatibles UK , Ltd., Farnham, GB
DecisionSubstantially Equivalent, Dec 11, 2015
ReceivedAug 3, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K152157

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.