Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K934303
›
Descendants
Devices descending from K934303
3 later devices reach RFA A-300 through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K011763
Omnidos
Scanditronix Medical AB
2001
1
—
+1
K961400
Rfa-300, Lda Utility
Scanditronix Medical AB
1997
2
—
+2
K092018
Omnipro Incline
Iba Dosimetry GmbH
2009
0
—