K250884
- 510(k) number
- K250884
- Device name
- 0.9 % Sodium Chloride Injection, USP, BD PosiFlush SP Syringe
- Applicant
- Becton, Dickinson and Company NJ · US
- Product code
- NGT — Saline, Vascular Access Flush
- Decision date
- 2025-12-02
- Date received
- 2025-03-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250884.pdf
Official FDA record: K250884
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.