# K003495: Ancure Lliac Balloon Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Guidant Cardiac and Vascular Surgery
- Decided: Feb 7, 2001 after 86 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.
28 later devices descend from it; 3 cite it directly.
0 of 29 devices in its family (counting itself) have 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
- K032869: Cook Coda Balloon Catheter (2003), 26 descendants of its own
- K122917: Coda Balloon Catheter (2013), 11 descendants of its own
- K050038: Reliant Stent Graft Balloon Catheter (2005), 11 descendants of its own
- K150970: Coda LP Balloon Catheter (2015), 10 descendants of its own
- K151821: ER-REBOA Catheter (2015), 9 descendants of its own

Source page: https://510kreport.com/device/K003495
Methodology: https://510kreport.com/methodology