K232388
- 510(k) number
- K232388
- Device name
- High Pressure Tubing
- Applicant
- Ningbo Dizegens Medical Science Co.,Ltd CN
- Product code
- DXT — Injector And Syringe, Angiographic
- Decision date
- 2023-11-21
- Date received
- 2023-08-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232388.pdf
Official FDA record: K232388
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.