Home / Companies / Aidera AB

Aidera AB

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K101806AIDERA DIASEND SYSTEMDecember 7, 2010
K083221AIDERA DIASENDFebruary 3, 2009