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Mobilemedtek
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Medical Device Manufacturer
·
US , Louisville , KY
Mobilemedtek - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2017
Recent clearances:
ElectroTek
View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mobilemedtek
Neurology
✕
1
devices
1-1 of 1
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Cleared
Jun 05, 2017
ElectroTek
K170441
·
GWQ
Neurology
·
111d
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