ClearanceBrief
510(k) K233069 ยท PUR Vacuum Syringe

Removal System Large Bore 60 cc Syringe

ApplicantInari Medical, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Mar 26, 2024
ReceivedSep 26, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233069

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.