510(k) K233021 · LHI Set, I.V. Fluid Transfer
BD SmartSite 13mm Vial Access Device; BD SmartSite 20mm Vial Access Device
| Applicant | Care Fusion, San Diego CA, US |
| Decision | Substantially Equivalent, Mar 6, 2024 |
| Received | Sep 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233021
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.