# K972110: Cordis Endeavor Infusion Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Aug 14, 1997 after 70 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.
13 later devices descend from it; 1 cites it directly.
0 of 14 devices 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) Cordis Infusion Catheters (3.0 - 3.5 mm): named in the summary without a submission number
- (no number) SciMed Dispatch Gold Infusion Catheters: named in the summary without a submission number

## Most influential descendants
- K063620: Ekos Micro-Infusion System (2007), 12 descendants of its own
- K073166: Endowave Infusion System (2008), 11 descendants of its own
- K081467: Ekosonic Endovascular System with Rapid Pulse Modulation (2008), 10 descendants of its own
- K111705: Ekosonic Endovascular System (2011), 9 descendants of its own
- K183290: Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 (2019), 8 descendants of its own

## 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/K972110
Methodology: https://510kreport.com/methodology