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510k Database
Manufacturers
US
Euromi S.A
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Medical Device Manufacturer
·
US , Huntington , CT
Euromi S.A - FDA 510(k) Cleared Devices
2 submissions
·
2 cleared
·
Since 2001
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Euromi S.A
General & Plastic Surgery
✕
2
devices
1-2 of 2
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Cleared
Dec 16, 2010
EUROMI EVA SP6
K101413
·
QPB
General & Plastic Surgery
·
210d
Cleared
Jun 29, 2001
LIPOMATIC
K010311
·
QPB
General & Plastic Surgery
·
148d
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General & Plastic Surgery
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