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510k Database
Manufacturers
US
Diotech CO
Medical Device Manufacturer
·
US , Pittsburgh , PA
Diotech CO - FDA 510(k) Cleared Devices
2 submissions
·
2 cleared
·
Since 2014
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Diotech CO
General & Plastic Surgery
✕
2
devices
1-2 of 2
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Cleared
Jun 09, 2016
ATOVEN-Reusable Laser Fiber
K152667
·
GEX
General & Plastic Surgery
·
266d
Cleared
Aug 26, 2014
DIOTECH LASER FIBER
K140458
·
GEX
General & Plastic Surgery
·
183d
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General & Plastic Surgery
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