# K230196: syngo.via View&GO VA40A

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Healthcare GmbH
- Decided: Feb 13, 2023 after 19 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: 15 generations back to K913770 (1991). 185 ancestors in all.
1 later device descends from it; 1 cites it directly.
3 of 187 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221501: syngo.via View&GO, Siemens Healthcare GmbH (2022) Summary page 5.

## Most influential descendants
- K252634: Imagine® Enterprise Suite (2026), 0 descendants of its own

## Indications for use
syngo.via View&GO is indicated for image rendering and post-processing of DICOM images to support the interpretation in the field of radiology, nuclear medicine and cardiology. The system is not indicated for mammography images for diagnosis in the U.S. The application is not to be used as an archiving device for patients’ image data. The application is not to be used as a sole basis for clinical decisions but further evidence has to be taken into account.

Source page: https://510kreport.com/device/K230196
Methodology: https://510kreport.com/methodology