# K083127: Asahi Corsair Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Asahi Intecc Co., Ltd.
- Decided: Feb 3, 2009 after 105 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). 13 ancestors in all.
33 later devices descend from it; 6 cite it directly.
0 of 47 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062885: Stride Microcatheter, Asahi Intecc Co., Ltd. (2007) Summary page 1.
- K051772: Asahi Tornus Support Catheter, Asahi Intecc Co., Ltd. (2005) Summary page 1.
- K050599: Tracker Excel -14 Pre-Shaped Microcatheter, Boston Scientific Corp (2005) Summary page 1.

## Most influential descendants
- K151103: ASAHI Corsair Microcatheter (2015), 20 descendants of its own
- K161126: ASAHI Corsair Pro (2016), 11 descendants of its own
- K112035: Valet Micro Catheter (2012), 9 descendants of its own
- K171933: ASAHI PTCA Guide Wires, ASAHI Corsair Microcatheter, ASAHI Corsair Pro Microcatheter (2018), 7 descendants of its own
- K141649: Spex Support Catheter (2014), 6 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/K083127
Methodology: https://510kreport.com/methodology