# K142065: Turnpike Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Vascular Solutions, Inc.
- Decided: Nov 25, 2014 after 118 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 K001992 (2000). 16 ancestors in all.
4 later devices descend from it; 3 cite it directly.
1 of 21 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091345: Gopher Gold Catheter, Model 5620, Vascular Solutions, Inc. (2009) Summary page 4.
- K051772: Asahi Tornus Support Catheter, Asahi Intecc Co., Ltd. (2005) Summary page 4.

## Most influential descendants
- K151981: Turnpike catheter (2015), 2 descendants of its own
- K191560: Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter (2019), 1 descendant of its own
- K260559: NHanceIT (2026), 0 descendants of its own
- K214106: QuikPass Catheter (2022), 0 descendants of its own

## Indications for use
Turnpike catheter is intended to be used to access discrete regions of the coronary and/or peripheral vasculature. It may be used to facilitate placement and exchange of guidewires and to subselectively infuse/deliver diagnostic and therapeutic agents.

Source page: https://510kreport.com/device/K142065
Methodology: https://510kreport.com/methodology