# K955801: Radifocus Glidewire GT with Gold Coil,Glidewire Gold

- Pathway: 510(k) (Traditional)
- Applicant: Terumo Medical Corp.
- Decided: Feb 2, 1996 after 42 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.
15 later devices descend from it; 2 cite it directly.
0 of 16 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
- K080863: Traxcess 0.014 Hydrophilic Guidewire (2008), 12 descendants of its own
- K133725: Traxcess 14 Guidewire (2014), 9 descendants of its own
- K153053: Traxcess Pro 14 Guidewire (2015), 4 descendants of its own
- K161803: Traxcess .007 Mini Guidewire (2016), 2 descendants of its own
- K182337: HYBRID Guidewire (2018), 1 descendant of its own

Source page: https://510kreport.com/device/K955801
Methodology: https://510kreport.com/methodology