# K101479: Wingman Extendable Tip Support Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Reflow Medical
- Decided: Aug 11, 2010 after 75 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). 18 ancestors in all.
5 later devices descend from it; 1 cites it directly.
2 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001577: Outback Catheter, Lumend, Inc. (2001)
- K072750: Spectranetics Quick-Cross SUPPORT2 Catheters, Models 518-065 and 518-066, Spectranetics Corp. (2007) Summary page 1.
- K091345: Gopher Gold Catheter, Model 5620, Vascular Solutions, Inc. (2009) Summary page 1.

## Most influential descendants
- K120178: Wingman Extendable Tip Support Catheter (2012), 4 descendants of its own
- K132420: Wingman Extendable Tip Support Catheter (2013), 3 descendants of its own
- K141547: Wingman Extendable Tip Support Catheter (2014), 2 descendants of its own
- K173661: Wingman 35 Crossing Catheter (2018), 0 descendants of its own
- K151880: Wingman Crossing Catheter (2015), 0 descendants of its own

## Indications for use
The Wingman Extendable Tip Support Catheter is intended to be used in conjunction with steerable guidewires to access discreet regions of the peripheral 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/K101479
Methodology: https://510kreport.com/methodology