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912
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Polymer Patient Examination Glove
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510k Database
Manufacturers
DE
Robodent GmbH
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Medical Device Manufacturer
·
DE , Berlin
Robodent GmbH - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2006
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Robodent GmbH
Neurology
✕
1
devices
1-1 of 1
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Cleared
Sep 05, 2006
LAPDOC I
K061224
·
HAW
Neurology
·
127d
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