# K141782: HI-Torque Versaturn Guide Wire

- Pathway: 510(k) (Special)
- Applicant: Abbott Vascular
- Decided: Aug 7, 2014 after 36 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: 6 generations back to K913353 (1991). 12 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K103101: HI-Torque Balance Middleweight Elite, Abbott Vascular-Cardiac Therapies (2011) Summary page 4.

## Most influential descendants
- K173795: HI-TORQUE TurnTrac Guide Wire Family (2018), 0 descendants of its own

## Indications for use
The HI-TORQUE VersaTurn Guide Wire Family is intended to facilitate the delivery of catheter-based interventional devices during percutaneous transluminal angioplasty (PTA) and percutaneous transluminal coronary angioplasty (PTCA). This guide wire may also be used with compatible stent devices during therapeutic procedures. This device is designed and intended for ONE-TIME USE ONLY. Do not resterilize and / or reuse.

Source page: https://510kreport.com/device/K141782
Methodology: https://510kreport.com/methodology