# K222083: LimFlow V-Ceiver

- Pathway: 510(k) (Traditional)
- Applicant: LimFlow, Inc.
- Decided: Aug 9, 2022 after 25 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: 7 generations back to K901502 (1990). 16 ancestors in all.
1 later device descends from it; 1 cites it directly.
2 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112185: Foursnare Vascular Retrieval Snare, Cook, Inc. (2011) Summary page 4.

## Most influential descendants
- K242776: LimFlow V-Ceiver (2025), 0 descendants of its own

## Indications for use
The LimFlow V-Ceiver™ is intended for use in the cardiovascular system to manipulate and retrieve guidewires specified in the IFU.

Source page: https://510kreport.com/device/K222083
Methodology: https://510kreport.com/methodology