K233277
- 510(k) number
- K233277
- Device name
- Filter Needle for Single Use
- Applicant
- Hangzhou Qiantang Longyue Biotechnology Co., Ltd. CN
- Product code
- FPB — Filter, Infusion Line
- Decision date
- 2024-05-10
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K233277.pdf
Official FDA record: K233277
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.