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510k Database
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US
Oktx, LLC
Medical Device Manufacturer
·
US , Tulsa , OK
Oktx, LLC - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2013
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Oktx, LLC
Neurology
✕
1
devices
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Cleared
Sep 13, 2013
PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)
K123902
·
IKN
Neurology
·
269d
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Neurology
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