K232055
- 510(k) number
- K232055
- Device name
- Vial Adapter
- Applicant
- Shanghai Lingfu Technology Co., Ltd. CN
- Product code
- LHI — Set, I.V. Fluid Transfer
- Decision date
- 2023-10-06
- Date received
- 2023-07-11
- 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: K232055.pdf
Official FDA record: K232055
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.