# K904404: Multi-Lumen Central Venous Catheter Set

- Pathway: 510(k) (Traditional)
- Applicant: Arrow Intl., Inc.
- Decided: Feb 15, 1991 after 143 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
62 later devices descend from it; 3 cite it directly.
1 of 63 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K032274: Cook Five Lumen Central Venous Catheter (2004), 33 descendants of its own
- K060174: Spectrum Five Lumen Central Venous Catheter Set, Model C-UQLM10.0-Abrm (2006), 32 descendants of its own
- K081113: Cook and Cook Spectrum Central Venous Catheters (2008), 31 descendants of its own
- K012512: Setpoint Endovascular Temperature Management System (2002), 27 descendants of its own
- K101326: NMI IC (2010), 26 descendants of its own

Source page: https://510kreport.com/device/K904404
Methodology: https://510kreport.com/methodology