# K971019: Chase Vessel Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Chase Medical, Inc.
- Decided: Jul 21, 1997 after 123 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 K760624 (1976). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K760624: Small Vessel Cannula, Cobe Laboratories, Inc. (1976) Summary page 1.

## Indications for use
The Vessel Cannula is indicated for use during open-heart surgery to perfuse fluid into vein grafts.

Source page: https://510kreport.com/device/K971019
Methodology: https://510kreport.com/methodology