# K203842: Bendit21 Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Bend IT Technologies, Ltd.
- Decided: Apr 13, 2022 after 468 days
- Product code: QJP (Catheter, Percutaneous, Neurovasculature)
- 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.
1 later device descends from it; 1 cites it directly.
0 of 8 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.

## Most influential descendants
- K252213: Bendit17 Microcatheter (2025), 0 descendants of its own

## Indications for use
The Bendit®21 Microcatheter is intended for use in accessing target locations in the peripheral, coronary, and neuro vasculature and can be used to deliver both diagnostic agents, such as contrast media, and therapeutic devices. Use only contrast media and therapeutic devices that have been cleared or approved for use in the intended target area.

Source page: https://510kreport.com/device/K203842
Methodology: https://510kreport.com/methodology