K260301
- 510(k) number
- K260301
- Device name
- Vial Adapter
- Applicant
- Hangzhou Qiantang Longyue Biotechnology Co., Ltd. CN
- Product code
- LHI — Set, I.V. Fluid Transfer
- Decision date
- 2026-06-05
- Date received
- 2026-01-30
- 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: K260301.pdf
Official FDA record: K260301
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.