# K052775: Syngo Multimodality Workplace (Syngo MM WP)

- Pathway: 510(k) (Traditional)
- Applicant: Siemens AG Medical Solutions
- Decided: Oct 31, 2005 after 28 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
181 later devices descend from it; 1 cites it directly.
1 of 182 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K061964: Syngo Multimodality Workplace (2006), 180 descendants of its own
- K072728: Syngo Multimodality Workplace (2008), 178 descendants of its own
- K081734: Syngo Imaging (Version V31) (2008), 177 descendants of its own
- K092519: Syngo.X (2009), 176 descendants of its own
- K112020: Syngo.CT Vascular Analysis (2011), 99 descendants of its own

## Recalls of this device
- Nov 13, 2008 · Not classified · Z-0647-2009: Indicated orientation does not match actual orientation of the patient.

Source page: https://510kreport.com/device/K052775
Methodology: https://510kreport.com/methodology