K232577
- 510(k) number
- K232577
- Device name
- Radial Compression Device
- Applicant
- Ningbo Dizegens Medical Science Co.,Ltd NJ · US
- Product code
- DXC — Clamp, Vascular
- Decision date
- 2024-01-18
- Date received
- 2023-08-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232577.pdf
Official FDA record: K232577
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.