# K160848: Wingman 18 Crossing Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Reflow Medical, Inc.
- Decided: Jul 14, 2016 after 108 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). 17 ancestors in all.
3 later devices descend from it; 1 cites 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.
- K072750: Spectranetics Quick-Cross SUPPORT2 Catheters, Models 518-065 and 518-066, Spectranetics Corp. (2007) Summary page 4.

## Most influential descendants
- K170996: Wingman 14C Crossing Catheter (2017), 2 descendants of its own
- K190393: Wingman 14C Crossing Catheter (2019), 1 descendant of its own
- K210188: coraCross (2021), 0 descendants of its own

## Indications for use
The Wingman 18 Crossing Catheter is intended to be used in conjunction with steerable guidewires to access discreet regions of the peripheral and/or coronary vasculature. It may be used to facilitate placement and exchange of guidewires and other interventional devices and provide a conduit for the delivery of saline solutions or diagnostic/therapeutic agents.

Source page: https://510kreport.com/device/K160848
Methodology: https://510kreport.com/methodology