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510k Database
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US
Anthrotronix, Inc.
Medical Device Manufacturer
·
US , Silver Spring , MD
Anthrotronix, Inc. - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2014
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Anthrotronix, Inc.
Neurology
✕
1
devices
1-1 of 1
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Cleared
Oct 15, 2014
DANA
K141865
·
LQD
Neurology
·
97d
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Neurology
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