K231071
- 510(k) number
- K231071
- Device name
- Mix2Vial® Transfer Device
- Applicant
- West Pharma. Services IL, Ltd. IL
- Product code
- LHI — Set, I.V. Fluid Transfer
- Decision date
- 2024-01-19
- Date received
- 2023-04-14
- 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: K231071.pdf
Official FDA record: K231071
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.