# K123311: Qxmedical Access & Support Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Qxmedical, LLC
- Decided: Jan 14, 2013 after 81 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
Longest line of descent: 6 generations back to K935425 (1994). 12 ancestors in all.
4 later devices descend from it; 3 cite it directly.
1 of 17 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082337: Minnie Support Catheter, Vascular Solutions, Inc. (2009) Summary page 1.
- K033678: Spectranetics Quick Cross Catheters, Models 518-032, 518-033, 518034, 518-035, 518-036, 518-037 and 518-038, Spectranetics Corp. (2004) Summary page 1.

## Most influential descendants
- K170041: XableCath Support Catheter (2017), 1 descendant of its own
- K200317: Support Catheter (2020), 0 descendants of its own
- K180986: XableCath Support Catheter Product Family (2018), 0 descendants of its own
- K160561: Boosting Catheter (2016), 0 descendants of its own

## Indications for use
The Access & Support Catheter is intended for use during coronary and peripheral interventional procedures to guide and support guidewires, traverse discrete portions of the vasculature, allow for guidewire exchanges and provide a conduit for infusion of saline solution, diagnostic contrast agents and therapeutic agents.

Source page: https://510kreport.com/device/K123311
Methodology: https://510kreport.com/methodology