# K150422: EOPA 3D Arterial Cannula

- Pathway: 510(k) (Special)
- Applicant: Medtronic, Inc.
- Decided: Mar 20, 2015 after 29 days
- Product code: DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K840002 (1984). 8 ancestors in all.
1 later device descends 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)
- K061254: Eopa 3D Arterial Cannula, Models 78220,78222,78320,783222, Medtronic Perfusion Systems (2006) Summary page 5.

## Most influential descendants
- K260195: Elongated One-Piece Arterial (EOPA) 3D™ Arterial Cannulae (2026), 0 descendants of its own

## Indications for use
These cannulae are intended for use in perfusion of the ascending aorta during short term (6 hours or less) cardiopulmonary bypass.

Source page: https://510kreport.com/device/K150422
Methodology: https://510kreport.com/methodology