ClearanceBrief
510(k) K220301 ยท FPA Set, Administration, Intravascular

Volumat Line

ApplicantFresenius Kabi, Bad Hersfeld, DE
DecisionSubstantially Equivalent, Jun 2, 2023
ReceivedFeb 2, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220301

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.