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Optovent AB
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Medical Device Manufacturer
·
US , Fort Lee , NJ
Optovent AB - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2001
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Optovent AB
Anesthesiology
✕
1
devices
1-1 of 1
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Cleared
Feb 05, 2001
OPTOVENT RESPONS, OPTOVENT RENEE (OPTOVENT RESPONS WITHOUT PULSE OXIMETRY...
K003704
·
BZQ
Anesthesiology
·
66d
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