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Eurospital
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Medical Device Manufacturer
·
US , Beverly , MA
Eurospital - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2000
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Eurospital
General Hospital
✕
1
devices
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Cleared
Feb 29, 2000
SECURMIX
K000367
·
LHI
General Hospital
·
25d
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General Hospital
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