K242429
- 510(k) number
- K242429
- Device name
- CentroVena Central Venous Catheter (CVC) with the CentroVena One Insertion System
- Applicant
- Becton Dickinson Inc. (Bd) UT · US
- Product code
- SEF — Central Venous Catheter With Manual Insertion System
- Decision date
- 2025-04-09
- Date received
- 2024-08-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K242429.pdf
Official FDA record: K242429
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.