ClearanceBrief
510(k) K143015 ยท FPA Set, Administration, Intravascular

Hospira Primary Sets

ApplicantHospira, Inc., Lake Forest IL, US
DecisionSubstantially Equivalent, Feb 25, 2015
ReceivedOct 20, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K143015

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.