Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K242342
›
Descendants
Devices descending from K242342
2 later devices reach Fetal EchoScan through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K252294
Fetal EchoScan (v1.2)
Brightheart
2025
0
—
+1
K251071
Fetal EchoScan (v1.1)
Brightheart
2025
1
—