MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE
Jul 1991
88d
Stortz
1
Total
1
Cleared
0
Denied
Stortz — FDA 510(k) Submissions
Stortz has submitted 1 FDA 510(k) premarket notifications since 1991, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Unit, Examining/treatment, Ent . Use the specialty filter in the sidebar to narrow results.
1 devices