Cello Partnership D/B/A Verizon Wireless is one of 5184 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cello Partnership D/B/A Verizon Wireless - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Cello Partnership D/B/A Verizon Wireless has 1 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cello Partnership D/B/A Verizon Wireless Filter by specialty or product code using the sidebar.
Cello Partnership D/B/A Verizon Wireless — FDA 510(k) Products and Clearance History
1 devices