# K151103: ASAHI Corsair Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Asahi Intecc Co., Ltd.
- Decided: Jun 23, 2015 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: 7 generations back to K001992 (2000). 14 ancestors in all.
20 later devices descend from it; 5 cite it directly.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083127: Asahi Corsair Microcatheter, Asahi Intecc Co., Ltd. (2009) Summary page 4.

## Most influential descendants
- K161126: ASAHI Corsair Pro (2016), 11 descendants of its own
- K171933: ASAHI PTCA Guide Wires, ASAHI Corsair Microcatheter, ASAHI Corsair Pro Microcatheter (2018), 7 descendants of its own
- K152249: ASAHI Corsair Armet (2016), 3 descendants of its own
- K182360: Teleport Microcatheter (2018), 2 descendants of its own
- K161362: ASAHI Corsair Armet (2016), 2 descendants of its own

## Indications for use
The ASAHI Corsair Microcatheter is intended to provide support to facilitate the placement of Guide wires in the coronary and peripheral vasculatures and can be used to exchange one guide wire for another. The Corsair Microcatheter is also intended to assist in the delivery of contrast media into the coronary, peripheral, and abdominal vasculatures.

Source page: https://510kreport.com/device/K151103
Methodology: https://510kreport.com/methodology