# K083094: Streamer Polymer Guidewire

- Pathway: 510(k) (Traditional)
- Applicant: Brivant, Ltd.
- Decided: Jul 7, 2009 after 263 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: 6 generations back to K970376 (1997). 17 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060551: Brivant Guidewire, Brivant Limited (2006) Summary page 1.
- K030019: Modification to HI-Torque Whisper Guidewire, Guidant Corp. (2003)

## Most influential descendants
- K103377: Charter Guidewire Model 45-281, 45-282, 45-283 (2011), 2 descendants of its own
- K141831: Hydraview Guidewire (2014), 0 descendants of its own
- K122856: Charter Guidewire (2012), 0 descendants of its own

## Indications for use
The Streamer Polymer guide wires are intended for use in the coronary and peripheral vasculature to facilitate the selective placement of interventional catheters with compatible guidewire lumen and Biotronik coronary venous leads.

Source page: https://510kreport.com/device/K083094
Methodology: https://510kreport.com/methodology