# K090193: Conductor Coronary Guidewire

- Pathway: 510(k) (Traditional)
- Applicant: Concert Medical, LLC
- Decided: Sep 25, 2009 after 241 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: 4 generations back to K913353 (1991). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001736: Galeo Hydro and Galeo Hydro J-Tip, Biotronik, Inc. (2000)
- K982272: Galeo HS 014 Model 117 130, Galeo S 014 Model 115 488, Galeao M 014 Model 114156, Galeo F 014 Model 115 487 Galeo HF 018, Biotronik, Inc. (1999) Summary page 1.

## Indications for use
For use in vascular interventional procedures to facilitate placement of catheters within the coronary arteries.

Source page: https://510kreport.com/device/K090193
Methodology: https://510kreport.com/methodology