K231888
- 510(k) number
- K231888
- Device name
- BD Texium Needle-Free Syringe
- Applicant
- Care Fusion CA · US
- Product code
- FMF — Syringe, Piston
- Decision date
- 2023-09-25
- Date received
- 2023-06-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K231888.pdf
Official FDA record: K231888
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.