# K062062: Voyager Pacs System

- Pathway: 510(k) (Traditional)
- Applicant: Voyager Imaging
- Decided: Sep 11, 2006 after 53 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- 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 K010259 (2001). 4 ancestors in all.
5 later devices descend from it; 5 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060263: Iqpacs, S.C. Info World S.R.L. (2006) Summary page 1.

## Most influential descendants
- K102148: Curiepacs (Dicom Pacs Software) (2010), 0 descendants of its own
- K093247: Medsynapse Pacs Software (2009), 0 descendants of its own
- K082240: Sntrypacs (2008), 0 descendants of its own
- K081752: Edge Pacs (2008), 0 descendants of its own
- K071602: Imagic V2.0 (2007), 0 descendants of its own

## Indications for use
Voyager PACS System' TM is a software based device that receives digital images and data from various sources (i.e. CT scanners, MR scanners, ultrasound systems, R/F Units, computed & direct radiographic devices, secondary capture devices, scanners, imaging gateways, etc.). Images and data can be captured, stored, communicated, processed and displayed within the system and or across computer networks at distributed locations. Lossy compressed mammographic images and digitized film screen images must not be reviewed for primary image interpretation. Mammographic images may only be interpreted using an FDA approved monitor that offers at least 5 Mpixel resolution and meets other technical specifications reviewed and accepted by FDA.

Source page: https://510kreport.com/device/K062062
Methodology: https://510kreport.com/methodology