# K192402: syngo.CT Extended Functionality

- Pathway: 510(k) (Special)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Sep 20, 2019 after 17 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K971684 (1997). 133 ancestors in all.
4 later devices descend from it; 1 cites it directly.
3 of 138 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K173625: syngo.CT Clinical Extensions, Siemens Medical Solutions USA, Inc. (2018) Summary page 5.
- K150757: syngo.CT Dual Energy, Siemens Medical Solutions USA, Inc. (2015) Summary page 5.

## Most influential descendants
- K203699: syngo. CT Extended Functionalities (2021), 3 descendants of its own
- K214019: syngo.CT Extended Functionality (2022), 1 descendant of its own
- K221727: syngo.CT Extended Functionality (2022), 0 descendants of its own
- K213096: Al-Rad Companion (Pulmonary) (2021), 0 descendants of its own

## Indications for use
syngo.CT Extended Functionality is intended to provide advanced visualization tools to prepare and process medical images for diagnostic purpose. The software package is designed to support technicians and physicians in qualitative and quantitative measurements and in the analysis of clinical data that was acquired and reconstructed by Computed Tomography (CT) scanners, and possibly other medical imaging modalities (e.g. MR scanners). An interface shall enable the connection between the syngo.CT Extended Functionality software package and the interconnected CT Scanner system. Result images created with the syngo.CT Extended Functionality software package can be used to assist trained technicians or physicians in diagnosis.

Source page: https://510kreport.com/device/K192402
Methodology: https://510kreport.com/methodology