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510k Database
Manufacturers
SE
Toul Meditech AB
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Medical Device Manufacturer
·
SE , V?ster?s
Toul Meditech AB - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 2016
Recent clearances:
SteriStay
,
Operio
,
Operio
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Toul Meditech AB
General & Plastic Surgery
✕
1
devices
1-1 of 1
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Cleared
May 10, 2019
SteriStay
K190027
·
ORC
General & Plastic Surgery
·
123d
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General Hospital
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General & Plastic Surgery
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