# K970914: Chase Aortic Perfusion Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Chase Medical, Inc.
- Decided: May 13, 1997 after 62 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: 1 generation back to K770429 (1977). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K770429: Cannulae, Aortic, Arch, High Flow, 3M Health Care, Sarns (1977) Summary page 1.
- K790565: Aortic Root Cannula, Dlp, Inc. (1979) Summary page 1.
- (no number) aortic cross clamp: named in the summary without a submission number

## Indications for use
The Aortic Perfusion Cannula is indicated for use for perfusion of the ascending aorta during surgical procedures requiring cardiopulmonary bypass. Additionally, the Aortic Perfusion Cannula can be used to occlude the ascending aorta as well as deliver cardioplegia solution to and aspirate air from the aorta.

Source page: https://510kreport.com/device/K970914
Methodology: https://510kreport.com/methodology