K252040
- 510(k) number
- K252040
- Device name
- BD Vacutainer® Plasma Separator Tubes (PST), BD Vacutainer® Sodium Heparin Blood Collection Tubes
- Applicant
- Becton, Dickinson and Company NJ · US
- Product code
- JKA — Tubes, Vials, Systems, Serum Separators, Blood Colle
- Decision date
- 2026-03-13
- Date received
- 2025-06-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Chemistry
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K252040.pdf
Official FDA record: K252040
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.