# K200266: BD Centro Vena Acute Central Line (7 French Dual Lumen)

- Pathway: 510(k) (Special)
- Applicant: Bard Access Systems, Inc. (Bard Has Joined Bd)
- Decided: Apr 7, 2020 after 64 days
- Product code: FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K001901 (2000). 25 ancestors in all.
No later device cites it as a predicate yet.
4 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K190855: BD Acute Central Line, Bard Access Systems, Inc. (Bard Has Joined Bd) (2019) Summary page 5.

## Indications for use
Acute central venous catheters are indicated to provide short-term access (<30 days) to the central venous system. They are designed for administering I.V. fluids, blood products, drugs and parenteral nutrition solutions, as well as blood withdrawal, central venous pressure monitoring, and power injection of contrast media.

Source page: https://510kreport.com/device/K200266
Methodology: https://510kreport.com/methodology