# K971041: Chase Coronary Ostial Perfusion Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Chase Medical, Inc.
- Decided: May 13, 1997 after 53 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Medtronic/DLP Coronary Ostial Perfusion Cannula: named in the summary without a submission number

## Indications for use
The Coronary Ostial Perfusion Cannula is intended for use in conjunction with cardiopulmonary bypass surgery for delivery of cardioplegia solutions directly to the coronary arteries.

Source page: https://510kreport.com/device/K971041
Methodology: https://510kreport.com/methodology