NOVAPROBE LED LIGHT SOURCE
Jul 2014
450d
Novaprobe Incorporated
1
Total
1
Cleared
0
Denied
Novaprobe Incorporated — FDA 510(k) Submissions
Novaprobe Incorporated has submitted 1 FDA 510(k) premarket notifications since 2014, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Light Source, Fiberoptic, Routine . Use the specialty filter in the sidebar to narrow results.
1 devices