Medical Device Manufacturer · US , Elk Grove Village , IL

Miegmbh - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2010
4
Total
4
Cleared
0
Denied

FDA 510(k) cleared devices by Miegmbh Radiology ✕

4 devices
1-4 of 4
Cleared Aug 27, 2020
ANCORIS
K201807 · KPS
Radiology · 57d
Cleared Apr 19, 2013
ECAT SCINTRON PET
K130269 · KPS
Radiology · 74d
Cleared Oct 05, 2010
MIE SCINTRON GAMMA CAMERA SYSTEMS
K101768 · KPS
Radiology · 104d
Cleared Jun 07, 2010
MODIFICATION TO SCINTRON IV
K101013 · KPS
Radiology · 56d
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