Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K211096
›
Descendants
Devices descending from K211096
2 later devices reach Optiflow Oxygen Kit through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K262268
Optiflow Oxygen Kit (AA484J)
Fisher and Paykel Healthcare Limited
2026
0
—
+1
K233821
F&P Optiflow Oxygen Kit (AA451J)
Fisher & Paykel Healthcare, Ltd.
2024
0
—