X O ODONTOSURGE 4
Apr 2003
179d
Xo Care A/S
1
Total
1
Cleared
0
Denied
Xo Care A/S — FDA 510(k) Submissions
Xo Care A/S 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 Unit, Electrosurgical, And Accessories, Dental . Use the specialty filter in the sidebar to narrow results.
1 devices