# K232443: Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit

- Pathway: 510(k) (Special)
- Applicant: Argon Medical Devices, Inc.
- Decided: Sep 7, 2023 after 24 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: 8 generations back to K901502 (1990). 15 ancestors in all.
No later device cites it as a predicate yet.
1 of 16 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K191758: Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit, Argon Medical Devices, Inc. (2019) Summary page 4.

## Indications for use
Single-Loop Snare Retrieval Kit and Triple-Loop Snare Retrieval Kit are intended for the percutaneous removal of retrievable inferior vena cava (IVC) filters that are no longer medically required, via jugular approach.

Source page: https://510kreport.com/device/K232443
Methodology: https://510kreport.com/methodology