# K965181: Ces Infusion Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Neurovascular, Inc.
- Decided: Mar 21, 1997 after 87 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
83 later devices descend from it; 5 cite it directly.
0 of 84 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) TRANSIT® Infusion Catheter: named in the summary without a submission number
- (no number) RapidTRANSIT® Infusion Catheter: named in the summary without a submission number
- (no number) Tracker Infusion Catheters: named in the summary without a submission number

## Most influential descendants
- K972518: Transit/Rapidtransit/Speedster/Prowler Infusion Catheter (1997), 81 descendants of its own
- K020680: Prowler Select 10 and 14 Infusion Catheters with and Without Pre-Shaped Tips (2002), 35 descendants of its own
- K062885: Stride Microcatheter (2007), 34 descendants of its own
- K083127: Asahi Corsair Microcatheter (2009), 33 descendants of its own
- K151103: ASAHI Corsair Microcatheter (2015), 20 descendants of its own

## Indications for use
CES Infusion Catheters are intended to be used as a mechanism for the infusion of various diagnostic and embolic agents into the peripheral, coronary and neurovasculatures.

Source page: https://510kreport.com/device/K965181
Methodology: https://510kreport.com/methodology