# K962932: Cordis Stabilizer Plus XS

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Oct 25, 1996 after 88 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: 1 generation back to K935997 (1994). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K953760: Cordis Wizdom Steerable Guidewire, Cordis Corp. (1995) Summary page 1.
- K935997: Platinum Plus Guidewire, Boston Scientific Corp (1994) Summary page 1.
- (no number) Scimed/Boston Scientific Platinum Plus™ Coronary Guidewire: named in the summary without a submission number

## Indications for use
The Cordis STABILIZER Plus XS Steerable Guidewires are intended 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/K962932
Methodology: https://510kreport.com/methodology