# K113716: Asahi Chikai V Peripheral Vascular Guide Wire

- Pathway: 510(k) (Traditional)
- Applicant: Asahi Intecc Co., Ltd.
- Decided: Feb 6, 2012 after 49 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- 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 K890505 (1989). 10 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993257: .010 Silverspeed Hydropophilic Guidewire, .014 Silversped Hydrophilic Guidewire, .016 Silverspeed Hydrophilic Guidewi, Micro Therapeutics, Inc. (1999) Summary page 1.
- K110584: Asahi Chikai Neurovascular Guide Wire, Asahi Intecc Co., Ltd. (2011) Summary page 1.
- K022762: Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000, AG143000, AG141002, AG141010, AG14M060 & AG14M050, Jomed, Inc. (2002) Summary page 1.
- K971254: Transend EX Platinum Guidewire, Boston Scientific Corp (1997) Summary page 1.

## Most influential descendants
- K161584: ASAHI® Peripheral Vascular Guide Wire ASAHI Meister®16 (2016), 0 descendants of its own

## Indications for use
ASAHI Peripheral Vascular Guide Wire is intended for use in the peripheral vasculature, to facilitate the exchange and placement of diagnostic and therapeutic devices such as vascular catheters during peripheral interventional procedures. This guide wire is not intended for use in neuro- or coronary vasculature.

Source page: https://510kreport.com/device/K113716
Methodology: https://510kreport.com/methodology