ASEPTYLUM, UNI-CARRIER
Jun 1996
39d
Distriflor S.A.
1
Total
1
Cleared
0
Denied
Distriflor S.A. — FDA 510(k) Submissions
Distriflor S.A. has submitted 1 FDA 510(k) premarket notifications since 1996, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Burnisher, Operative . Use the specialty filter in the sidebar to narrow results.
1 devices