K234024
- 510(k) number
- K234024
- Device name
- HWJECT Auto-disable syringe
- Applicant
- Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. CN
- Product code
- FMF — Syringe, Piston
- Decision date
- 2024-03-19
- Date received
- 2023-12-20
- 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: K234024.pdf
Official FDA record: K234024
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.