Viztek, LLC is one of 18468 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Viztek, LLC - FDA 510(k) Cleared Devices
Recent clearances: ViZion DR + Wireless, ViZion DR + Wireless, EXA
6
Total
6
Cleared
0
Denied
Viztek, LLC has 6 FDA 510(k) cleared medical devices. Based in Naples, US.
Historical record: 6 cleared submissions from 2011 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Viztek, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Viztek, LLC
6 devices