# K953760: Cordis Wizdom Steerable Guidewire

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Nov 7, 1995 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
No predicates in its family tree.
6 later devices descend from it; 4 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K040592: Cordis Steer-IT Deflecting Tip Guidewire (2004), 2 descendants of its own
- K070212: CITOP10 Guidewire, 0.014(1.4MM Tip), CITOP6 Guidewire, 0.014(1.0MM Tip), Citop Support Accessory, 0.023(126CM) (2007), 1 descendant of its own
- K171897: Approach CTO Microwire Guide (2017), 0 descendants of its own
- K990823: PVS 1400 Guidewire (1999), 0 descendants of its own
- K963214: Cordis ST Steerable Guidewire (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K953760
Methodology: https://510kreport.com/methodology