510(k) K260128 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
BD Preset and BD A-Line Arterial Blood Collection Syringes
| Applicant | Becton, Dickinson and Company, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Apr 15, 2026 |
| Received | Jan 16, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K260128
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.