Medical Device Manufacturer · SE , Goteborg

Aidera AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Aidera AB General Hospital ✕

2 devices
1-2 of 2
Cleared Dec 07, 2010
AIDERA DIASEND SYSTEM
K101806 · MRZ
General Hospital · 162d
Cleared Feb 03, 2009
AIDERA DIASEND
K083221 · MRZ
General Hospital · 95d
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