# K242776: LimFlow V-Ceiver

- Pathway: 510(k) (Special)
- Applicant: LimFlow, Inc.
- Decided: Feb 14, 2025 after 154 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). 17 ancestors in all.
No later device cites it as a predicate yet.
2 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222083: LimFlow V-Ceiver, LimFlow, Inc. (2022) Summary page 5.

## 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/K242776
Methodology: https://510kreport.com/methodology