# K123223: EC Single Use, Polypectomy Snare

- Pathway: 510(k) (Traditional)
- Applicant: Endochoice, Inc.
- Decided: Jan 10, 2013 after 87 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: 1 generation back to K955650 (1996). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K955650: Olympus SD Series Snares, Olympus America, Inc. (1996) Summary page 1.

## Indications for use
The EC Single Use, Polypectomy Snare is indicated to endoscopically resect tissue from within the GI tract.

Source page: https://510kreport.com/device/K123223
Methodology: https://510kreport.com/methodology