# K060454: Titan Guidewire

- Pathway: 510(k) (Special)
- Applicant: Lake Region Mfg., Inc.
- Decided: Mar 24, 2006 after 30 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 K941895 (1994). 20 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052347: Titan Steerable (Ptca) Guidewire, Lake Region Mfg., Inc. (2006) Summary page 3.

## Most influential descendants
- K073655: Pegasus Steerable (Ptca) Guidewire (2008), 0 descendants of its own

## Indications for use
For use in angiographic procedures to introduce and position catheters and interventional devices within the coronary and peripheral vasculature.

Source page: https://510kreport.com/device/K060454
Methodology: https://510kreport.com/methodology