# K123024: Torque Device

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific Corporation
- Decided: Oct 26, 2012 after 28 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: 2 generations back to K951802 (1995). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K922706: Scimed Sideliner, Scimed (1992) Summary page 1.
- K120694: Encore 26 Advantage Kit, Boston Scientific Corp (2012) Summary page 1.

## Indications for use
The Torque Device is used for guidewire manipulation during general intravascular procedures.

Source page: https://510kreport.com/device/K123024
Methodology: https://510kreport.com/methodology