ClearanceBrief
510(k) K253235 · FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Introcan Safety® Deep Access XL IV Catheter

ApplicantB.Braun Medical, Inc., Bethlehem PA, US
DecisionSubstantially Equivalent, May 15, 2026
ReceivedSep 29, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253235

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.