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510k Database
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US
Oxypulse
Medical Device Manufacturer
·
US , Mesa , AZ
Oxypulse - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2010
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Oxypulse
Anesthesiology
✕
1
devices
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Cleared
Jun 16, 2010
OXIBLUE FINGERTIP PULSE OXIMETER MODEL MD300C318, OXIPRO FINGERTIP PULSE...
K100815
·
DQA
Anesthesiology
·
85d
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