# K260188: LimFlow Vector

- Pathway: 510(k) (Special)
- Applicant: LimFlow, Inc.
- Decided: Mar 18, 2026 after 55 days
- Product code: MGZ (Valvulotome)
- Device class: 2
- Regulation: 21 CFR 870.4885
- 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 K946352 (1995). 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)
- K221902: LimFlow Vector, LimFlow, Inc. (2022) Summary page 5.

## Indications for use
The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for excising or disrupting venous valves.

Source page: https://510kreport.com/device/K260188
Methodology: https://510kreport.com/methodology