# K970842: Cordis Endeavor Infusion Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: May 28, 1997 after 82 days
- Product code: QEY (Mechanical Thrombolysis Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- 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) SciMed Dispatch Infusion Catheter: named in the summary without a submission number
- (no number) SciMed Dispatch Gold Infusion Catheter: named in the summary without a submission number
- (no number) LocalMed InfusaSleeve Infusion Catheter: named in the summary without a submission number
- (no number) LocalMed InfusaSleeve II Infusion Catheter: named in the summary without a submission number
- (no number) Interventional Innovations Segue Infusion Catheter: named in the summary without a submission number

## Indications for use
The Cordis Endeavor Infusion Catheter is intended to deliver solutions, such as heparinized saline, and thrombolytic agents, such as urokinase, to the coronary and peripheral vasculature.

Source page: https://510kreport.com/device/K970842
Methodology: https://510kreport.com/methodology