# K132652: Via Microcatheter, Via Plus Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Sequent Medical, Inc.
- Decided: Dec 20, 2013 after 116 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K960806 (1996). 9 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091559: Marksmann Catheter, Chestnut Medical Technologies, Inc. (2009) Summary page 1.
- K113778: Excelsior XT-27 Microcatheter, Stryker Neurovascular (2012) Summary page 3.
- K123477: Via Microcatheter, Via Plus Microcatheter, Sequent Medical, Inc. (2013) Summary page 1.

## Most influential descendants
- K150894: VIA 21 Microcatheter (2015), 2 descendants of its own
- K162565: VIA 17 Microcatheter (2017), 1 descendant of its own
- K192135: VIA Microcatheter (size 17), VIA Microcatheter (size 21), VIA Microcatheter (size 27), VIA Microcatheter (size 33) (2019), 0 descendants of its own

## Recalls of this device
- Sep 23, 2016 · Class II · Z-0114-2017: Sequent Medical is recalling the VIA 27 Microcatheter because it may not adequately re-sheath the interventional device into the catheter as designed.

## Indications for use
The VIATh Micracatheter is intended for the introduction of non-liquid interventional devices (such as stents/flow, diverters) and infusion of diagnostic (such as contrast media), or therapeutic agents into the neuro, peripheral and coronary vasculature.

Source page: https://510kreport.com/device/K132652
Methodology: https://510kreport.com/methodology