# K023351: Magic Infusion Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Interventional Technologies, LLC
- Decided: Feb 20, 2003 after 136 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
Longest line of descent: 1 generation back to K923368 (1993). 1 ancestor in all.
22 later devices descend from it; 2 cite it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K923368: Magic Infusion Catheter, Target Therapeutics (1993) Summary page 1.

## Most influential descendants
- K041826: Ekos Ultrasound Infusion System (2005), 19 descendants of its own
- K051225: Ekos Micro-Infusion System (2005), 18 descendants of its own
- K053437: Ekos Micro-Infusion System (2006), 16 descendants of its own
- K053432: Ekos Micro-Infusion System (2005), 16 descendants of its own
- K062508: Neurowave Micro-Infusion System (2006), 14 descendants of its own

## Indications for use
The Magic Infusion Catheter is intended for regional infusion of contrast materials into selected vessels in the neurovasculature. The Magic Infusion Catheter may be used for controlled, regional infusion into selected vessels and is not intended for use in the coronary vasculature.

Source page: https://510kreport.com/device/K023351
Methodology: https://510kreport.com/methodology