Nuvon, Inc. is one of 5253 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nuvon, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Nuvon, Inc. has 2 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.
Historical record: 2 cleared submissions from 2010 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Nuvon, Inc. Filter by specialty or product code using the sidebar.
Nuvon, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Mar 13, 2013
NUVON VITALS CHARTING SYSTEM
Cardiovascular
42d
Cleared
Oct 22, 2010
VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM
General Hospital
85d