LIGHT GUIDE CABLE
Nov 2011
196d
Schott North America
1
Total
1
Cleared
0
Denied
Schott North America — FDA 510(k) Submissions
Schott North America has submitted 1 FDA 510(k) premarket notifications since 2011, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Illuminator, Fiberoptic, Surgical Field . Use the specialty filter in the sidebar to narrow results.
1 devices