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510k Database
Manufacturers
US
Ksea
Medical Device Manufacturer
·
US , Culver City , CA
Ksea - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2006
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ksea
Gastroenterology & Urology
✕
1
devices
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Cleared
Aug 21, 2006
KSEA BIPOLAR ELECTROTOME
K061541
·
FAS
Gastroenterology & Urology
·
77d
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Gastroenterology & Urology
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