# K973845: Cordis Hydronol Steerable Guidewire

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Jan 5, 1998 after 89 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Terumo Radifocus Glidewire: named in the summary without a submission number
- (no number) LRM Steerable Hydrophilic Guidewire: named in the summary without a submission number

## Most influential descendants
- K014195: Kayak Hydrophilic Guide Wires (2002), 0 descendants of its own

## Indications for use
The Cordis Hydronol Steerable Guidewires are designed for use in angiographic procedures to introduce and position catheters and interventional devices within the peripheral vasculature.

Source page: https://510kreport.com/device/K973845
Methodology: https://510kreport.com/methodology