# K063877: Syngo Lung Cad

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Oct 18, 2006 after 6 days
- Product code: OEB (Lung Computed Tomography System, Computer-Aided Detection)
- 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
No predicates in its family tree.
19 later devices descend from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K143196: syngo.CT Lung CAD (2015), 18 descendants of its own
- K163341: syngo.CT Extended Functionality (2017), 6 descendants of its own
- K193216: syngo.CT Lung CAD (2020), 5 descendants of its own
- K173625: syngo.CT Clinical Extensions (2018), 5 descendants of its own
- K161201: ClearRead CT (2016), 5 descendants of its own

Source page: https://510kreport.com/device/K063877
Methodology: https://510kreport.com/methodology