SOVIS OPTIQUE'S ENDOSCOPIC CABLE
Dec 2002
63d
Sovis Optique
1
Total
1
Cleared
0
Denied
Sovis Optique — FDA 510(k) Submissions
Sovis Optique has submitted 1 FDA 510(k) premarket notifications since 2002, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Image, Illumination, Fiberoptic, For Endoscope . Use the specialty filter in the sidebar to narrow results.
1 devices