# K141831: Hydraview Guidewire

- Pathway: 510(k) (Traditional)
- Applicant: Brivant Limited
- Decided: Sep 4, 2014 after 59 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K970376 (1997). 20 ancestors in all.
No later device cites it as a predicate yet.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083094: Streamer Polymer Guidewire, Brivant, Ltd. (2009) Summary page 4.
- K103377: Charter Guidewire Model 45-281, 45-282, 45-283, Brivant, Ltd. (2011) Summary page 4.

## Indications for use
The HydraView Polymer Guidewires are intended for use in the coronary and peripheral vasculature to facilitate the selective placement of interventional devices with compatible guidewire lumen and compatible coronary venous leads.

Source page: https://510kreport.com/device/K141831
Methodology: https://510kreport.com/methodology