# K060174: Spectrum Five Lumen Central Venous Catheter Set, Model C-UQLM10.0-Abrm

- Pathway: 510(k) (Special)
- Applicant: Cook, Inc.
- Decided: Feb 17, 2006 after 25 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: 3 generations back to K960764 (1997). 8 ancestors in all.
32 later devices descend from it; 1 cites it directly.
1 of 41 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032274: Cook Five Lumen Central Venous Catheter, Cook, Inc. (2004)
- K033843: Spectrum Central Venous Catheter with or Without Hydrophilic Coating, Cook, Inc. (2004)
- K962577: Arrowgard Blue Quad-Lumen Central Venous Catheter, Arrow Intl., Inc. (1997) Summary page 2.
- K010021: Medcomp Quad Lumen, 8.5F X 20CM, Model MC4L-8S, Medical Components, Inc. (2001)

## Most influential descendants
- K081113: Cook and Cook Spectrum Central Venous Catheters (2008), 31 descendants of its own
- K101326: NMI IC (2010), 26 descendants of its own
- K121089: Nmi Picc Iii (2012), 23 descendants of its own
- K111906: Xcela Hybrid Picc with Pasv Valve Technology (2011), 14 descendants of its own
- K122882: Nmi Hpicc Iii (2012), 12 descendants of its own

## Indications for use
The Spectrum Five Lumen Central Venous Catheter Set is indicated for the intravenous administration of nutrients, fluids, chemotherapeutic agents, and other drugs for therapy, blood sampling, blood delivery, and venous pressure monitoring.

Source page: https://510kreport.com/device/K060174
Methodology: https://510kreport.com/methodology