# K071204: Site-Rite 6 Ultrasound System, Model Site-Rite 6

- Pathway: 510(k) (Special)
- Applicant: C.R. Bard, Inc.
- Decided: May 18, 2007 after 17 days
- Product code: IYO (System, Imaging, Pulsed Echo, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K850478 (1985). 5 ancestors in all.
136 later devices descend from it; 5 cite it directly.
0 of 142 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052517: Site-Rite 5 Ultrasound System, C.R. Bard, Inc. (2005) Summary page 1.

## Most influential descendants
- K142443: Site-Rite 6 Ultrasound System with Pinpoint GT Technology (2014), 64 descendants of its own
- K092619: Etrax Needle System, Etrax Variable Angle Needle Guidance System, Virtutrax Universal Tracker (2009), 61 descendants of its own
- K152758: Venue 50 (2015), 55 descendants of its own
- K160277: LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 (2016), 47 descendants of its own
- K161706: Vivid iq (2016), 46 descendants of its own

## Indications for use
The Site-Rite®6 UltrasoundSystem with associatedprobe and accessoriesprovide ultrasound guidancefor placement of needles and catheters in vascular structures. Ultrasoundguidance may occur intraoperativelyor percutaneously. Ultrasoundimaging of vascular structures, various organs and structures of the body may also be performed

Source page: https://510kreport.com/device/K071204
Methodology: https://510kreport.com/methodology