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510k Database
Manufacturers
US
Angiotech
Medical Device Manufacturer
·
US , Herndon , VA
Angiotech - FDA 510(k) Cleared Devices
7 submissions
·
6 cleared
·
Since 2007
7
Total
6
Cleared
1
Denied
FDA 510(k) Regulatory Record - Angiotech
Gastroenterology & Urology
✕
2
devices
1-2 of 2
Filters
Cleared
Jan 24, 2008
SKATER BILIARY CATHETER
K073672
·
FGE
Gastroenterology & Urology
·
28d
Cleared
Jun 21, 2007
SKATER BILIARY CATHETER
K070610
·
FGE
Gastroenterology & Urology
·
108d
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7
General & Plastic Surgery
4
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2
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