# K180795: JUDO 1 Guidewire, JUDO 3 Guidewire, JUDO 6 Guidewire

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific
- Decided: Apr 12, 2018 after 16 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). 22 ancestors in all.
No later device cites it as a predicate yet.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K152231: Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire, Boston Scientific Corporation (2016) Summary page 4.

## Indications for use
Boston Scientific JUDO 1, JUDO 3, and JUDO 6 Guidewires are intended to facilitate the placement of balloon dilatation catheters or other interventional therapeutic devices during percutaneous transluminal coronary angioplasty (PTCA) or other intravascular interventional procedures. These guidewires are not intended for use in the cerebral vasculature,

Source page: https://510kreport.com/device/K180795
Methodology: https://510kreport.com/methodology