# K200120: LiteSaber Wire Torque Assist Device

- Pathway: 510(k) (Traditional)
- Applicant: Vesatek, LLC
- Decided: May 7, 2020 after 107 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: 9 generations back to K854261 (1985). 18 ancestors in all.
No later device cites it as a predicate yet.
1 of 19 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170684: Firebow Wire Torque Assist Device, Vesatek, LLC (2017) Summary page 4.

## Indications for use
The LiteSaber WTAD is used to maneuver guidewires in the coronary and peripheral vasculature during interventional or diagnostic procedures. The LiteSaber WTAD is not intended for use in the neurovasculature.

Source page: https://510kreport.com/device/K200120
Methodology: https://510kreport.com/methodology