K222780
- 510(k) number
- K222780
- Device name
- LILY Extension Tube and Needleless Connector
- Applicant
- Lily Medical Corporation CN
- Product code
- FPA — Set, Administration, Intravascular
- Decision date
- 2023-11-09
- Date received
- 2022-09-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K222780.pdf
Official FDA record: K222780
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.