# K072728: Syngo Multimodality Workplace

- Pathway: 510(k) (Traditional)
- Applicant: Siemens AG Medical Solutions
- Decided: Apr 22, 2008 after 209 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: 5 generations back to K971684 (1997). 12 ancestors in all.
178 later devices descend from it; 3 cite it directly.
1 of 191 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061964: Syngo Multimodality Workplace, Siemens AG Medical Solutions (2006) Summary page 3.

## Most influential descendants
- K092519: Syngo.X (2009), 176 descendants of its own
- K112020: Syngo.CT Vascular Analysis (2011), 99 descendants of its own
- K123920: Syngo.Via (2013), 63 descendants of its own
- K093621: Syngo.Pet&CT Oncology (2010), 54 descendants of its own
- K150843: syngo®.via (version VB10A) (2015), 46 descendants of its own

## Indications for use
The syngo MultiModality Workplace is intended to be used for viewing, manipulation, communication, and storage of medical images and data exchange media. The syngo MultiModality Workplace can be used as a stand-alone device or as with a variety of cleared and unmodified syngo- and Windows XP-based software options. The syngo MultiModality Workplace does not support the display of mammography images for diagnosis.

Source page: https://510kreport.com/device/K072728
Methodology: https://510kreport.com/methodology