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2017
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1152
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947
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818
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795
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788
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740
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724
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699
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510k Database
Manufacturers
US
S.S. Ent.
Medical Device Manufacturer
·
US , Weston , CT
S.S. Ent. - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1992
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - S.S. Ent.
Gastroenterology & Urology
✕
1
devices
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Cleared
Apr 20, 1992
VIVAMED FISTULA NEEDLE
K903440
·
FIE
Gastroenterology & Urology
·
629d
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Gastroenterology & Urology
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