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510k Database
Manufacturers
US
Summit TO Sea
Medical Device Manufacturer
·
US , Mound , MN
Summit TO Sea - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2008
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Summit TO Sea
Anesthesiology
✕
1
devices
1-1 of 1
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Cleared
Feb 08, 2008
DIVE AND SHALLOW AND GRAND DIVE
K072757
·
CBF
Anesthesiology
·
134d
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Anesthesiology
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