Realtimeimage, Inc. is one of 23674 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Realtimeimage, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IPACS PRISM-5.0, IPACS CARDIO, IPACS ORTHO
4
Total
4
Cleared
0
Denied
Realtimeimage, Inc. has 4 FDA 510(k) cleared medical devices. Based in Denton, US.
Historical record: 4 cleared submissions from 2003 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Realtimeimage, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Realtimeimage, Inc.
4 devices