# K123922: Syngo Dynamics

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Jan 16, 2013 after 27 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: 8 generations back to K842308 (1984). 30 ancestors in all.
5 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)
- K102150: Syngo Dynamics, Version 9.0, Siemens Medical Solutions USA, Inc. (2010) Summary page 6.

## Most influential descendants
- K171053: syngo Dynamics Version VA30 (2017), 4 descendants of its own
- 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/K123922
Methodology: https://510kreport.com/methodology