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570
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523
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522
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Polymer Patient Examination Glove
489
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475
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Intervertebral Fusion Device...
436
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Screw, Fixation, Bone
404
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US
Biover AG
Medical Device Manufacturer
·
US , Ridley Park , PA
Biover AG - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2002
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biover AG
Cardiovascular
✕
1
devices
1-1 of 1
Filters
Cleared
Oct 02, 2002
BIOVER
K011208
·
DXC
Cardiovascular
·
531d
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Cardiovascular
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