K260128
- 510(k) number
- K260128
- Device name
- BD Preset and BD A-Line Arterial Blood Collection Syringes
- Applicant
- Becton, Dickinson and Company NJ · US
- Product code
- JKA — Tubes, Vials, Systems, Serum Separators, Blood Colle
- Decision date
- 2026-04-15
- Date received
- 2026-01-16
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Clinical Chemistry
510(k) Summary (official FDA PDF): K260128.pdf
Official FDA record: K260128
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.