# K091345: Gopher Gold Catheter, Model 5620

- Pathway: 510(k) (Special)
- Applicant: Vascular Solutions, Inc.
- Decided: Jun 12, 2009 after 37 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: 6 generations back to K001992 (2000). 15 ancestors in all.
20 later devices descend from it; 4 cite it directly.
2 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070372: Gopher 2F Support Catheter, Model 5600 and Gopher 3F Support Catheter, Model 5610, Vascular Solutions, Inc. (2007) Summary page 1.

## Most influential descendants
- K101479: Wingman Extendable Tip Support Catheter (2010), 5 descendants of its own
- K142065: Turnpike Catheter (2014), 4 descendants of its own
- K120178: Wingman Extendable Tip Support Catheter (2012), 4 descendants of its own
- K101659: Supercross Microcatheter (130 CM), Supercross Microcatheter (150 CM) Model 5300, 5301 (2010), 4 descendants of its own
- K160848: Wingman 18 Crossing Catheter (2016), 3 descendants of its own

## Indications for use
The Gopher Gold catheter is intended to be used in conjunction with steerable guidewires to access discreet regions of the coronary and/or peripheral vasculature. It may be used to facilitate placement and exchange of guidewires and other interventional devices and to subselectively infuse/deliver diagnostic and therapeutic agents.

Source page: https://510kreport.com/device/K091345
Methodology: https://510kreport.com/methodology