RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGER
Aug 2010
125d
Acceletronics Digital Imaging, LLC
1
Total
1
Cleared
0
Denied
Acceletronics Digital Imaging, LLC — FDA 510(k) Submissions
Acceletronics Digital Imaging, LLC has submitted 1 FDA 510(k) premarket notifications since 2010, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Simulation, Radiation Therapy . Use the specialty filter in the sidebar to narrow results.
1 devices