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632
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621
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528
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522
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Polymer Patient Examination Glove
490
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485
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Intervertebral Fusion Device...
451
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443
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510k Database
Manufacturers
US
Adicon
Medical Device Manufacturer
·
US , Walker , MI
Adicon - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1982
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Adicon
General & Plastic Surgery
✕
1
devices
1-1 of 1
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Cleared
Dec 28, 1982
OPERATING ROOM PROCEDURAL PACK
K822804
General & Plastic Surgery
·
102d
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General & Plastic Surgery
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