Sanovas, Inc. is one of 15069 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sanovas, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PulmoVia Working Channel
1
Total
1
Cleared
0
Denied
Sanovas, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Rafael, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Sanovas, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Icon Plc as regulatory consultant.
FDA 510(k) Regulatory Record - Sanovas, Inc.
1 devices