ClearanceBrief
510(k) K132413 ยท FPA Set, Administration, Intravascular

MZ1000

ApplicantCare Fusion, San Diego CA, US
DecisionSubstantially Equivalent, Aug 29, 2013
ReceivedAug 2, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132413

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.