# K111079: Syngo.Via Web Viewer

- Pathway: 510(k) (Traditional)
- Applicant: Siemens AG Medical Solutions
- Decided: May 13, 2011 after 25 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: 7 generations back to K971684 (1997). 25 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092519: Syngo.X, Siemens AG Medical Solutions (2009) Summary page 3.
- K062673: Modification to Syngo Inspace 4D, Siemens AG Medical Solutions (2006) Summary page 3.

## Most influential descendants
- K130998: Syngo.Via Web Viewer (2014), 0 descendants of its own

## Indications for use
syngo.via WebViewer is intended to be a software-only solution for reviewing medical images from syngo.via. The system cannot be used as stand-alone device. It is intended to be an option for syngo.via system only. syngo.via WebViewer is not intended for storage or distribution of medical images from one medical device to another. syngo.via WebViewer is a client server architecture and the client is intended to run on web clients which are connected to the healthcare institution IT infrastructure where the customer has to ensure HIPPA compliance. syngo.via WebViewer supports interpretation and evaluation of examinations within healthcare institutions, for example, in Radiology, Nuclear Medicine and Cardiology environments. The communication of syngo.via WebViewer with connected medical IT systems will be done via standard interfaces such as but not limited to DICOM. The system is not intended for the displaying of digital mammography images for diagnosis in the U.S

Source page: https://510kreport.com/device/K111079
Methodology: https://510kreport.com/methodology