# K962676: Disposable Endoscopic Retrieval Device

- Pathway: 510(k) (Traditional)
- Applicant: United States Endoscopy Group, Inc.
- Decided: Oct 4, 1996 after 87 days
- Product code: FGO (Dislodger, Stone, Flexible)
- Device class: 2
- Regulation: 21 CFR 876.4680
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Recalls of this device
- Mar 10, 2015 · Class II · Z-1453-2015: A wire component on the distal grasping assembly of the device became detached..
- Nov 14, 2011 · Class II · Z-0006-2013: When the outer catheter is either coiled or in a contorted configuration outside of the endoscope and the patient, and excessive force is applied to the handle, the jaws may become inoperable and may 

Source page: https://510kreport.com/device/K962676
Methodology: https://510kreport.com/methodology