DETECTAR, MODEL N123-MI
Jun 2003
260d
Neks Technologies
1
Total
1
Cleared
0
Denied
Neks Technologies — FDA 510(k) Submissions
Neks Technologies has submitted 1 FDA 510(k) premarket notifications since 2003, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Handle, Instrument, Dental . Use the specialty filter in the sidebar to narrow results.
1 devices