ClearanceBrief
510(k) K142433 ยท FPA Set, Administration, Intravascular

Hospira Extension Set

ApplicantHospira, Inc., Lake Forest IL, US
DecisionSubstantially Equivalent, Dec 8, 2014
ReceivedAug 29, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142433

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.