Convergent Life Sciences, Inc. is one of 19008 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Convergent Life Sciences, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TARGET3D FUSION
1
Total
1
Cleared
0
Denied
Convergent Life Sciences, Inc. has 1 FDA 510(k) cleared medical devices. Based in Gold River, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Convergent Life Sciences, 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 - Convergent Life Sciences, Inc.
1 devices