# K962765: Cordis Marker Wire Steerable Guidewire (Stabilizer with Radiopaque Markers) and (Wizdom with Radiopaque Markers)

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Feb 21, 1997 after 220 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 K941269 (1994). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K952067: Cordis Steerable Guidewire, Cordis Corp. (1995) Summary page 1.
- K953750: Catheter, Electrode Recording, or Probe, Electrode Recording, Boston Scientific Corp (1996) Summary page 1.
- K941269: Gore Smoother II and Gore BPTB, W. L. Gore & Associates, Inc. (1994) Summary page 1.
- (no number) Rulers and Calipers: named in the summary without a submission number

## Most influential descendants
- K993248: Amplatzer Sizing Balloon (2000), 1 descendant of its own
- K053440: Amplatzer Sizing Balloon II (2005), 0 descendants of its own

## Indications for use
The Cordis STABILIZER Marker Wire Steerable Guidewire and Cordis WIZDOM Marker Wire Steerable Guidewire 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/K962765
Methodology: https://510kreport.com/methodology