# K192083: Okami Medical LOBO Vascular Occlusion System

- Pathway: 510(k) (Traditional)
- Applicant: Okami Medical
- Decided: Oct 30, 2019 after 89 days
- Product code: KRD (Device, Vascular, For Promoting Embolization)
- Device class: 2
- Regulation: 21 CFR 870.3300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K260508: LOBO Vascular Occlusion System (2026), 0 descendants of its own

## Indications for use
Intended Use: The Okami Medical LOBO Vascular Occlusion System is intended for use to obstruct or reduce the rate of blood flow in arteries of the peripheral vasculature. The device is not indicated for use in blood vessels where crush or bend forces are anticipated (e.g. joint areas, superficial vasculature).

Source page: https://510kreport.com/device/K192083
Methodology: https://510kreport.com/methodology