# K240426: Aventus Clot Management System

- Pathway: 510(k) (Traditional)
- Applicant: Inquis Medical
- Decided: May 14, 2024 after 91 days
- Product code: CAC (Apparatus, Autotransfusion)
- Device class: 2
- Regulation: 21 CFR 868.5830
- 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 K951592 (1996). 6 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K210176: FlowSaver Blood Filter, Inari Medical (2021) Summary page 5.

## Most influential descendants
- K253925: Aventus Thrombectomy System (2026), 2 descendants of its own
- K261105: Powered Aventus Thrombectomy System™ (2026), 0 descendants of its own
- K262030: Aventus Thrombectomy System (2026), 0 descendants of its own

## Indications for use
The Aventus Clot Management System is indicated for use with the Aventus Thrombectomy System for autologous blood transfusion.

Source page: https://510kreport.com/device/K240426
Methodology: https://510kreport.com/methodology