# K072526: Micrus Courier Enzo Microcatheter 0.0190

- Pathway: 510(k) (Special)
- Applicant: Micrus Endovascular Corporation
- Decided: Oct 5, 2007 after 28 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K960806 (1996). 9 ancestors in all.
5 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070456: Micrus Courier Enzo Microcatheter 0.017, Micrus Endovascular Corporation (2007) Summary page 1.

## Most influential descendants
- K161921: SwiftNINJA Microcatheter (2016), 4 descendants of its own
- K190126: Bendit2.7 Steerable Microcatheter (2019), 2 descendants of its own
- K200582: Bendit2.7 Steerable Microcatheter (2020), 1 descendant of its own
- K211110: Agile Devices Angler Steerable, Deflectable Microcatheter (2022), 0 descendants of its own
- K211525: SwiftNINJA Steerable Microcatheter (2021), 0 descendants of its own

## Indications for use
The Micrus Courier microcatheters are intended to assist in the delivery of diagnostic agents, such as contrast media, and therapeutic agents, such as occlusion coils, into peripheral, coronary, and neuro vasculature.

Source page: https://510kreport.com/device/K072526
Methodology: https://510kreport.com/methodology