# K963171: Cinch QR SGW Extension

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Nov 7, 1996 after 85 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 K914863 (1991). 1 ancestor in all.
1 later device descends 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)
- K914863: Cordis Cinch (R) Steerable Guidewire Ext W/SLX Coat, Cordis Corp. (1991) Summary page 1.

## Most influential descendants
- K093822: Docking Station,Teirstein Edge,Angioassist Combination Device, Angioassist Family (2010), 0 descendants of its own

## Indications for use
The Cordis CINCH® QR Steerable Guidewire Extension is designed to extend Cordis Steerable Guidewires so that a catheter can be exchanged for another catheter

Source page: https://510kreport.com/device/K963171
Methodology: https://510kreport.com/methodology