# K200317: Support Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Qxmedical, LLC
- Decided: May 14, 2020 after 97 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: 7 generations back to K935425 (1994). 13 ancestors in all.
No later device cites it as a predicate yet.
1 of 14 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123311: Qxmedical Access & Support Catheter, Qxmedical, LLC (2013) Summary page 4.

## Indications for use
The 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/K200317
Methodology: https://510kreport.com/methodology