CentroVena Central Venous Catheter (CVC) with the CentroVena One Insertion System— 510(k) K242429
Substantially EquivalentBecton Dickinson Inc. (Bd)
FDA 510(k) clearance K242429 for CentroVena Central Venous Catheter (CVC) with the CentroVena One Insertion System, Substantially Equivalent on 2025-04-09. Applicant: Becton Dickinson Inc. (Bd). Device class: 2.
Clearance details
- Applicant
- Becton Dickinson Inc. (Bd)
- Product code
- Code SEF
- Device class
- Class 2
- Regulation
- 21 CFR 880.5200
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake Ciy,, UT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.