# K123067: Progress Guide Wire Family, Pilot Guide Wire Family

- Pathway: 510(k) (Traditional)
- Applicant: Abbott Vascular, Inc.
- Decided: Jan 29, 2013 after 120 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). 14 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091825: HI-Torque Progress Guide Wire Family, Abbott Vascular, Inc. (2009) Summary page 1.
- K030549: HI-Torque Pilot 50 Guide Wire with Hydrocoat Hydrophilic Coating, HI-Torque Pilot 150 Guide Wire with Hydrocoat Hydrophg, Guidcorp (2003) Summary page 1.
- K101116: HI-Torque Pilot 50 and 150 Guide Wire with Hydrocoat Hydrophilic Coating, HI-Torque Whisper LS and MS Guide Wire with, Abbott Vascular-Cardiac Therapies (2010)

## Most influential descendants
- K193126: HI-TORQUE InfilTrac Guide Wire Family (2019), 1 descendant of its own
- K201834: HI-TORQUE PROCEED Guide Wire Family (2020), 0 descendants of its own

## Indications for use
Intended to facilitate the delivery of catheter-based interventional devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA). This guide wire may be used with compatible stent devices during therapeutic procedures. The guide wire may be used to reach and cross a target lesion, provide a pathway within the vessel structure, facilitate the substitution of one diagnostic or interventional device for another, and to distinguish the vasculature. This guide wire may also be used to cross or assist in crossing de nova chronic total coronary occlusions (CTO).

Source page: https://510kreport.com/device/K123067
Methodology: https://510kreport.com/methodology