# K171053: syngo Dynamics Version VA30

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Healthcare GmbH
- Decided: Jun 1, 2017 after 52 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: 9 generations back to K842308 (1984). 31 ancestors in all.
4 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)
- K123922: Syngo Dynamics, Siemens Medical Solutions USA, Inc. (2013) Summary page 4.

## Most influential descendants
- K220832: syngo Dynamics (Version VA40E) (2022), 3 descendants of its own
- 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 an image and information system intended for acceptance, transfer, display, storage, archive and manipulation of digital medical images, including review, analysis, quantification and reporting. As a Cardiology PACS and information system, syngo Dynamics supports the physician in interpretation and evaluation of examinations within healthcare institutions, in particular, in Cardiology, Obstetrics and Gynecology or other departments. syngo Dynamics is not intended to be used for displaying of digital mammography images for diagnosis in the U.S.

Source page: https://510kreport.com/device/K171053
Methodology: https://510kreport.com/methodology