# K093018: G-Prox Endoscopic Grasper, Model 205333

- Pathway: 510(k) (Special)
- Applicant: Usgi Medical
- Decided: Oct 7, 2009 after 29 days
- Product code: GAT (Suture, Nonabsorbable, Synthetic, Polyethylene)
- Device class: 2
- Regulation: 21 CFR 878.5000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K944415 (1994). 11 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061276: G-Prox Endoscopic Grasper, Usgi Medical (2006)

## Most influential descendants
- K103688: G-Prox EZ Endoscopic Grasper (2011), 0 descendants of its own

## Indications for use
The USGI g-Prox Endoscopic Grasper is intended for use in minimally invasive procedures to facilitate tissue grasping and manipulation.

Source page: https://510kreport.com/device/K093018
Methodology: https://510kreport.com/methodology