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US
Anodyne Corp.
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Medical Device Manufacturer
·
US , Brighton , MI
Anodyne Corp. - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1990
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Anodyne Corp.
General Hospital
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1
devices
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Cleared
Sep 12, 1990
ANOLIFT - PORTABLE & ANOLIFT - GANTRY
K902141
·
FSA
General Hospital
·
120d
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General Hospital
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