# K141547: Wingman Extendable Tip Support Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Reflow Medical
- Decided: Sep 30, 2014 after 111 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: 1 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K001992 (2000). 21 ancestors in all.
2 later devices descend from it; 2 cite 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)
- K132420: Wingman Extendable Tip Support Catheter, Reflow Medical (2013) Summary page 4.

## Most influential descendants
- K173661: Wingman 35 Crossing Catheter (2018), 0 descendants of its own
- K151880: Wingman Crossing Catheter (2015), 0 descendants of its own

## Recalls of this device
- Mar 22, 2017 · Class I · Z-1898-2017: ReFlow Medical is recalling the Wingman 35 Crossing Catheter because it may be prone to tip detachment.

## 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 mterventional devices and provide a conduit for the delivery of saline solutions or diagnostic/therapeutic agents.

Source page: https://510kreport.com/device/K141547
Methodology: https://510kreport.com/methodology