# K202366: MAGIC Infusion Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Balt USA, LLC
- Decided: Jan 29, 2021 after 163 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: 2 generations back to K923368 (1993). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023351: Magic Infusion Catheter, Advanced Interventional Technologies, LLC (2003) Summary page 4.

## Most influential descendants
- K213435: MAGIC Flow-Dependent Microcatheter (2022), 0 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/K202366
Methodology: https://510kreport.com/methodology