# K252213: Bendit17 Microcatheter

- Pathway: 510(k) (Special)
- Applicant: Bend IT Technologies, Ltd.
- Decided: Dec 3, 2025 after 141 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: 6 generations back to K960806 (1996). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K203842: Bendit21 Microcatheter, Bend IT Technologies, Ltd. (2022) Summary page 5.

## Indications for use
The Bendit17 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/K252213
Methodology: https://510kreport.com/methodology