# K041762: Finishing Wire Supportrak

- Pathway: 510(k) (Traditional)
- Applicant: Guidant Corporation
- Decided: Aug 6, 2004 after 37 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: 4 generations back to K002206 (2000). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K905674: Lead Stylet, Cardiac Pacemakers, Inc. (1991) Summary page 1.
- K023300: HI-Torque Whisper LS; HI-Torque Whisper MS; HI-Torque Whisper MS CS-J; HI-Torque Whisper ES; HI-Torque Whisper ES CS-J, Guidant Corp. (2002) Summary page 1.

## Indications for use
The SUPPORTRAK Finishing Wire is intended to aid in the placement of a Guidant implantable coronary venous lead in the coronary venous vasculature.

Source page: https://510kreport.com/device/K041762
Methodology: https://510kreport.com/methodology