# K221501: syngo.via View&GO

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Healthcare GmbH
- Decided: Oct 14, 2022 after 144 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: 14 generations back to K913770 (1991). 184 ancestors in all.
2 later devices descend 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)
- K201477: syngo.via View&GO, Siemens Healthcare GmbH (2020) Summary page 4.

## Most influential descendants
- K230196: syngo.via View&GO VA40A (2023), 1 descendant of its own
- 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.

Source page: https://510kreport.com/device/K221501
Methodology: https://510kreport.com/methodology