# K192135: VIA Microcatheter (size 17), VIA Microcatheter (size 21), VIA Microcatheter (size 27), VIA Microcatheter (size 33)

- Pathway: 510(k) (Traditional)
- Applicant: MicroVention, Inc.
- Decided: Dec 24, 2019 after 139 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K960806 (1996). 26 ancestors in all.
No later device cites it as a predicate yet.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150894: VIA 21 Microcatheter, Sequent Medical, Inc. (2015) Summary page 4.
- K132652: Via Microcatheter, Via Plus Microcatheter, Sequent Medical, Inc. (2013) Summary page 4.
- K162565: VIA 17 Microcatheter, Sequent Medical, Inc. (2017) Summary page 4.

## Recalls of this device
- Apr 21, 2021 · Class III · Z-1828-2021: Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.
- Apr 21, 2021 · Class III · Z-1830-2021: Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.
- Apr 21, 2021 · Class III · Z-1829-2021: Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.

## Indications for use
VIA 21, 27, 33 - The VIA® Microcatheter is intended for the introduction of interventional devices (such as the WEB device/stents/flow diverters) and infusion of diagnostic agents (such as contrast media) into the neuro, peripheral, and coronary vasculature. VIA 17, 17 Preshaped 45°, 17 Preshaped 90° - The VIA® Microcatheter is intended for the introduction of interventional devices (such as coils/stents) and infusion of diagnostic agents (such as contrast media) into the neuro, peripheral, and coronary vasculature.

Source page: https://510kreport.com/device/K192135
Methodology: https://510kreport.com/methodology