# K941973: Gip/Medi-Globe Guide Wires & Wind-UP Guide Wires

- Pathway: 510(k) (Traditional)
- Applicant: Medi-Globe Corp.
- Decided: Jun 30, 1995 after 434 days
- Product code: FGE (Stents, Drains And Dilators For The Biliary Ducts)
- Device class: 2
- Regulation: 21 CFR 876.5010
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K051068: Zutron Colonoscope Stiffening Device (2005), 1 descendant of its own
- K251204: FUJIFILM Stiffening Wire Device (SW-2000) (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K941973
Methodology: https://510kreport.com/methodology