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510k Database
Manufacturers
DE
Medovent GmbH
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Medical Device Manufacturer
·
DE , Mainz
Medovent GmbH - FDA 510(k) Cleared Devices
2 submissions
·
2 cleared
·
Since 2015
Recent clearances:
Reaxon Plus
,
Reaxon Plus
View 2 510(k) Devices ↓
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medovent GmbH
Neurology
✕
2
devices
1-2 of 2
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Cleared
Apr 24, 2018
Reaxon Plus
K180222
·
JXI
Neurology
·
89d
Cleared
Dec 02, 2015
Reaxon Plus
K143711
·
JXI
Neurology
·
338d
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Neurology
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