Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K123853
›
Descendants
Devices descending from K123853
3 later devices reach Vivasight-DL System through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K181886
VivaSight-DL System
Etview, Ltd.
2018
2
—
+2
K203749
Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable
Ambu A/S
2021
1
2
+3
K232529
Disposable Double Lumen Endobronchial Tube
Shenzhen Insighters Medical Technology Co., Ltd.
2024
0
—