# K182487: CerusEndo Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Cerus Endovascular, Inc.
- Decided: Jul 20, 2019 after 312 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K960806 (1996). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093160: Headway 21 Microcatheter, Model: MC212150S, MicroVention, Inc. (2009) Summary page 4.

## Indications for use
The CerusEndo Microcatheter is intended for general intravascular use to deliver therapeutic devices to the peripheral, coronary, and neurovasculature.

Source page: https://510kreport.com/device/K182487
Methodology: https://510kreport.com/methodology