# K192782: ASAHI CROSSWALK Peripheral Support Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Asahi Intecc Co., Ltd.
- Decided: Nov 29, 2019 after 60 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: 10 generations back to K001992 (2000). 17 ancestors in all.
No later device cites it as a predicate yet.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161362: ASAHI Corsair Armet, Asahi Intecc Co., Ltd. (2016) Summary page 4.

## Indications for use
The CROSSWALK™ Peripheral Support Catheter is intended to provide support to facilitate the placement of guide wires in the peripheral vasculature, and can be used to exchange one guide wire for another. The CROSSWALKTM Peripheral Support Catheter is also intended to assist in the delivery of contrast media into the peripheral vasculature.

Source page: https://510kreport.com/device/K192782
Methodology: https://510kreport.com/methodology