# K926104: Polyp Net

- Pathway: 510(k) (Traditional)
- Applicant: United States Endoscopy Group, Inc.
- Decided: Apr 5, 1993 after 123 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K122462: Roth Net Retriever (2012), 2 descendants of its own
- K152580: rescuenet (2015), 0 descendants of its own
- K142258: PolyCatch Retrieval Device (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K926104
Methodology: https://510kreport.com/methodology