# K914863: Cordis Cinch (R) Steerable Guidewire Ext W/SLX Coat

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Dec 18, 1991 after 50 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K963171: Cinch QR SGW Extension (1996), 1 descendant of its own
- K093822: Docking Station,Teirstein Edge,Angioassist Combination Device, Angioassist Family (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K914863
Methodology: https://510kreport.com/methodology