# K240205: Ez Catch Auto; Ez Catch YR; Ez Catch TR

- Pathway: 510(k) (Traditional)
- Applicant: Veol Medical Technologies Pvt, Ltd.
- Decided: Apr 15, 2024 after 81 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
Longest line of descent: 4 generations back to K060051 (2006). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K201243: Disposable Specimen Retrieval Bag, Beijing Biosis Healing Biolog Ical Technology Co., Ltd. (2020) Summary page 4.

## Indications for use
The device is indicated for use as a receptacle for the collection and extraction of tissue, organs and calculi during general and laparoscopic procedures.

Source page: https://510kreport.com/device/K240205
Methodology: https://510kreport.com/methodology