# K923368: Magic Infusion Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Target Therapeutics
- Decided: Apr 7, 1993 after 272 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.
26 later devices descend from it; 5 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K023351: Magic Infusion Catheter (2003), 22 descendants of its own
- 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

Source page: https://510kreport.com/device/K923368
Methodology: https://510kreport.com/methodology