Intelerad Medical Systems Incorporated is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Intelerad Medical Systems Incorporated - FDA 510(k) Cleared Devices
Recent clearances: IntelePACS
3
Total
3
Cleared
0
Denied
Intelerad Medical Systems Incorporated has 3 FDA 510(k) cleared medical devices. Based in Montreal, Qb, CA.
Historical record: 3 cleared submissions from 2009 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Intelerad Medical Systems Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O Tech, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Intelerad Medical Systems Incorporated
3 devices