# K142258: PolyCatch Retrieval Device

- Pathway: 510(k) (Traditional)
- Applicant: Medi-Globe Corporation
- Decided: Sep 30, 2014 after 47 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: 2 generations back to K926104 (1993). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122462: Roth Net Retriever, United States Endoscopy Group, Inc. (2012) Summary page 4.

## Indications for use
The PolyCatch Retrieval Device is intended for capture and retrieval of excised polyps, foreign bodies, tissue samples and calculi during flexible or rigid endoscopy procedures.

Source page: https://510kreport.com/device/K142258
Methodology: https://510kreport.com/methodology