Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K052288
›
Descendants
Devices descending from K052288
2 later devices reach Vitalogik through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K073140
Vitalogik Model 4000/4500
Mennen Medical, Ltd.
2007
0
—
+1
K070254
Horizon SE
Mennen Medical, Ltd.
2007
0
—