Radiology Information Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Radiology Information Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PowerDR
3
Total
3
Cleared
0
Denied
Radiology Information Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 3 cleared submissions from 1997 to 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Radiology Information Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Radiology Information Systems, Inc.
3 devices