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Sentinel
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Medical Device Manufacturer
·
US , Indianapolis , IN
Sentinel - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1991
View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sentinel
Anesthesiology
✕
1
devices
1-1 of 1
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Cleared
Feb 05, 1991
ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC
K904088
·
DQA
Anesthesiology
·
153d
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Anesthesiology
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