PVMED DDR 2520 DIGITAL IMAGING SYSTEM
Dec 2007
74d
Portavision Medical
1
Total
1
Cleared
0
Denied
Portavision Medical — FDA 510(k) Submissions
Portavision Medical has submitted 1 FDA 510(k) premarket notifications since 2007, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Imaging, X-ray, Electrostatic . Use the specialty filter in the sidebar to narrow results.
1 devices