K251350
- 510(k) number
- K251350
- Device name
- BD Plastipak Syringe
- Applicant
- Becton, Dickinson and Company NJ · US
- Product code
- FMF — Syringe, Piston
- Decision date
- 2025-07-29
- Date received
- 2025-04-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K251350.pdf
Official FDA record: K251350
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.