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510k Database
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US
Mivi, LLC
Medical Device Manufacturer
·
US , Maple Grove , MN
Mivi, LLC - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2014
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mivi, LLC
Cardiovascular
✕
1
devices
1-1 of 1
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Cleared
Sep 18, 2014
MIVI 6F GUIDE CATHETER
K140557
·
DQY
Cardiovascular
·
197d
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Cardiovascular
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