Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K062005
›
Descendants
Devices descending from K062005
3 later devices reach Portex Epidural Catheter through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K080140
Laurimed Spinal Injection System
Laurimed, LLC
2008
2
—
+2
K083909
Spinal Injection System
Laurimed, LLC
2009
1
—
+3
K091818
Laurimed Spinal Injection System
Laurimed, LLC
2009
0
—