K230235
- 510(k) number
- K230235
- Device name
- Medline Luer Lock Syringes
- Applicant
- Medline Industries, LP IL · US
- Product code
- FMF — Syringe, Piston
- Decision date
- 2024-02-16
- Date received
- 2023-01-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K230235.pdf
Official FDA record: K230235
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.