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510k Database
Manufacturers
DE
Optomotor Laboratories
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Medical Device Manufacturer
·
DE , D-79104 Freiburg
Optomotor Laboratories - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1999
Recent clearances:
EXPRESSEYE
View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Optomotor Laboratories
Neurology
✕
1
devices
1-1 of 1
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Cleared
Aug 12, 1999
EXPRESSEYE
K992473
·
GWN
Neurology
·
17d
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Neurology
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