ClearanceBrief
510(k) K231242 ยท BSO Catheter, Conduction, Anesthetic

Perifix FX Catheter; Contiplex FX Catheter

ApplicantB.Braun Medical, Inc., Center Valley PA, US
DecisionSubstantially Equivalent, Sep 15, 2023
ReceivedMay 1, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231242

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.