# K102484: Sequre Snare System

- Pathway: 510(k) (Traditional)
- Applicant: Lifetech Scientific (Shenzhen) Co., Ltd.
- Decided: Nov 9, 2010 after 71 days
- Product code: MMX (Device, Percutaneous Retrieval)
- Device class: 2
- Regulation: 21 CFR 870.5150
- 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 K901502 (1990). 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)
- K972511: Amplatz Goose Neck Snare Kit/ Catheter, Microvena Corp. (1998) Summary page 1.

## Indications for use
The SeQure™ Snare System is intended for use in the cardiovascular system as a tool to retrieve and manipulate foreign objects.

Source page: https://510kreport.com/device/K102484
Methodology: https://510kreport.com/methodology