K230287
- 510(k) number
- K230287
- Device name
- SaviSafe Safety Device
- Applicant
- Suzhou Savicred Biotechnology Co., Ltd. CN
- Product code
- MEG — Syringe, Antistick
- Decision date
- 2023-11-21
- Date received
- 2023-02-02
- 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: K230287.pdf
Official FDA record: K230287
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.