# K202252: ASAHI Corsair Armet 18 Microcatheter (Model: CSAR060-18N), ASAHI Corsair Armet 18 Microcatheter (Model: CSAR090-18N), ASAHI Corsair Armet 18 Microcatheter (Model: CSAR110-18N), ASAHI Corsair Armet 18 Microcatheter (Model: CSAR135-18N),

- Pathway: 510(k) (Special)
- Applicant: Asahi Intecc Co., Ltd.
- Decided: Sep 8, 2020 after 29 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 ASAHI Corsair Armet 18 is intended to provide support to facilitate the placement of guidewires in the peripheral vasculature, and can be used to exchange one guide wire for another. The ASAHI Corsair Armet 18 is also intended to assist in the delivery of contract media into the peripheral vasculature. This device should not be used in coronary vasculature or neurovasculature.

Source page: https://510kreport.com/device/K202252
Methodology: https://510kreport.com/methodology