# K062885: Stride Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Asahi Intecc Co., Ltd.
- Decided: Jun 13, 2007 after 260 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: 5 generations back to K001992 (2000). 12 ancestors in all.
34 later devices descend from it; 1 cites 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)
- K050599: Tracker Excel -14 Pre-Shaped Microcatheter, Boston Scientific Corp (2005) Summary page 1.
- K972518: Transit/Rapidtransit/Speedster/Prowler Infusion Catheter, Cordis Neurovascular, Inc. (1997) Summary page 1.
- K051772: Asahi Tornus Support Catheter, Asahi Intecc Co., Ltd. (2005) Summary page 1.

## Most influential descendants
- K083127: Asahi Corsair Microcatheter (2009), 33 descendants of its own
- 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

## Indications for use
The ASAHI Stride Microcatheter is intended to provide support to facilitate the placement of guide wires in the coronary and peripheral vasculature and can be used to exchange one guidewire for another. The Asahi Stride Microcatheter is also intended to assist in the delivery of diagnostic agents, such as contrast media and therapeutic agents, such as occlusion coils into the coronary and peripheral vasculature.

Source page: https://510kreport.com/device/K062885
Methodology: https://510kreport.com/methodology