# K091355: Deuce Polypectomy Snare, Models 000995, 000996,000997, 000998

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Endoscopic Technologies, Inc.
- Decided: Jul 22, 2009 after 75 days
- Product code: FDI (Snare, Flexible)
- Device class: 2
- Regulation: 21 CFR 876.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K894762 (1989). 12 ancestors in all.
No later device cites it as a predicate yet.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081580: Beamer Argon Snare Probe, Conmed Corporation (2008) Summary page 1.
- K050294: Cook Ireland Sonnet Polypectomy Snare, Cook Ireland, Ltd. (2005) Summary page 1.
- K943935: Gip/Medi-Globe Polypectomy Snares, Medi-Globe Corp. (1995) Summary page 1.
- K820430: Diathermic Snares, American Endoscopy, Inc. (1982) Summary page 1.

## Indications for use
May be used in conjunction with an electrosurgical generator for endoscopic resection of a polypoid lesion.

Source page: https://510kreport.com/device/K091355
Methodology: https://510kreport.com/methodology