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Sensocor
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Medical Device Manufacturer
·
US , Pompano Beach , FL
Sensocor - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1989
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sensocor
Cardiovascular
✕
1
devices
1-1 of 1
Filters
Cleared
Aug 03, 1989
SENSOCOR TM R-TEST 24OXL
K894234
·
DXG
Cardiovascular
·
44d
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Cardiovascular
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