Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K101403
›
Descendants
Devices descending from K101403
2 later devices reach Eli 250 Electrocardiograph through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K160840
ECG100+, ECG200+
Cardioline S.P.A
2016
0
—
+1
K122073
Eli 280 Electrocardiograph
Mortara Instrument, Inc.
2012
0
2