# K240384: SENDERO Microcatheter

- Pathway: 510(k) (Special)
- Applicant: Okami Medical, Inc.
- Decided: Mar 8, 2024 after 29 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: 9 generations back to K960806 (1996). 10 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K231600: SENDERO Microcatheter, Okami Medical, Inc. (2023) Summary page 4.

## Most influential descendants
- K242644: SENDERO MAX Delivery Catheter (2024), 0 descendants of its own

## Indications for use
The SENDERO Microcatheter is intended for the peripheral vasculature for the infusion of diagnostic and therapeutic agents.

Source page: https://510kreport.com/device/K240384
Methodology: https://510kreport.com/methodology