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510k Database
Manufacturers
FR
Sopro
Medical Device Manufacturer
·
FR , Marseille
Sopro - FDA 510(k) Cleared Devices
25 submissions
·
25 cleared
·
Since 1997
Recent clearances:
C50
Official Website
25
Total
25
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sopro
Radiology
✕
1
devices
1-1 of 1
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Cleared
Jul 20, 2010
SOPIX 2
K092329
·
MUH
Radiology
·
350d
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25
General & Plastic Surgery
13
Dental
6
Gastroenterology & Urology
3
Radiology
1
Obstetrics & Gynecology
1
Orthopedic
1