Vida Diagnostics, Inc. is one of 26046 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vida Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VIDAvision, VIDA PULMONARY WORKSTATION 2 (PW2)
2
Total
2
Cleared
0
Denied
Vida Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Iowa City, US.
Historical record: 2 cleared submissions from 2008 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Vida Diagnostics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Vida Diagnostics, Inc.
2 devices