# K182937: Upstream GoBack Crossing Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Upstream Peripheral Technologies, Ltd.
- Decided: May 23, 2019 after 213 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: 1 generation back to K001577 (2001). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 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) Summary page 4.

## Most influential descendants
- K211802: GoBack Crossing Catheter (2022), 0 descendants of its own

## Indications for use
The Upstream GoBack Crossing Catheter is intended to be used in conjunction with steerable guidewires to access discrete regions of the peripheral vasculature. It may be used to facilitate placement and exchange of guidewires. The Upstream GoBack Crossing Catheter is not intended for use in the coronary, cerebral or carotid vasculature.

Source page: https://510kreport.com/device/K182937
Methodology: https://510kreport.com/methodology