# K870825: New Model Styles for Aortic Arch Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Shiley, Inc.
- Decided: Mar 23, 1987 after 20 days
- Product code: DQR (Cannula, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K162215: Aortic Arch Cannulae, Optiflow Aortic Arch Cannulae (2017), 1 descendant of its own
- K180979: PureFlex Arterial Cannulae (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K870825
Methodology: https://510kreport.com/methodology