# K972993: Chase Femoral Access Cannulation Set

- Pathway: 510(k) (Traditional)
- Applicant: Chase Medical, Inc.
- Decided: Mar 31, 1998 after 231 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 K891576 (1989). 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)
- K891576: Fem-Flex Femoral Access Cannulation Set, Research Medical, Inc. (1989) Summary page 2.

## Indications for use
The Chase Medical Femoral Access Cannulation Set is intended for use in situations which require rapid femoral venous and arterial access for short term cardiopulmonary bypass. Venous and arterial access is left to the discretion of the physician.

Source page: https://510kreport.com/device/K972993
Methodology: https://510kreport.com/methodology