# K220832: syngo Dynamics (Version VA40E)

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: May 20, 2022 after 59 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: 10 generations back to K842308 (1984). 32 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171053: syngo Dynamics Version VA30, Siemens Healthcare GmbH (2017) Summary page 4.

## Most influential descendants
- K222428: Syngo Dynamics (Version VA40F) (2022), 2 descendants of its own
- K242551: syngo Dynamics (Version VA41D) (2025), 1 descendant of its own
- K253689: syngo Dynamics (VA41F) (2026), 0 descendants of its own

## Indications for use
syngo Dynamics is a multimodality, vendor agnostic Cardiology image and information system intended for medical image management and processing that provides capabilities relating to the review and digital processing of medical images. syngo Dynamics supports clinicians by providing post image processing functions for image manipulation, and/or quantification that are intended for use in the interpretation and analysis of medical images for disease detection, diagnosis, and/or patient management within the healthcare institution's network. syngo Dynamics is not intended to be used for display or diagnosis of digital mammography images in the U.S.

Source page: https://510kreport.com/device/K220832
Methodology: https://510kreport.com/methodology