ELEXOMA MEDIC
May 2008
464d
Redplane AG
1
Total
1
Cleared
0
Denied
Redplane AG — FDA 510(k) Submissions
Redplane AG has submitted 1 FDA 510(k) premarket notifications since 2008, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Cranial Electrotherapy Stimulator To Treat Insomnia And/or Anxiety . Use the specialty filter in the sidebar to narrow results.
1 devices