Intelerad Medical Systems, Inc. is one of 22890 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intelerad Medical Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INTELEPACS, INTELEPACS
2
Total
2
Cleared
0
Denied
Intelerad Medical Systems, Inc. has 2 FDA 510(k) cleared medical devices. Based in Denton, US.
Historical record: 2 cleared submissions from 2003 to 2007. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Intelerad Medical Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Intelerad Medical Systems, Inc.
2 devices