Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K173821
›
Descendants
Devices descending from K173821
3 later devices reach LungQ Software through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K232412
LungQ v3.0.0
Thirona BV
2024
1
—
+1
K212494
Lung Image Analysis
Pulmonx Corporation
2021
0
—
+2
K250766
LungQ 4
Thirona BV
2025
0
—