Intermed Advisors, Inc. is one of 25234 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intermed Advisors, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PATIENT DATA HANDLER & DEVICES (PDH&D)
1
Total
1
Cleared
0
Denied
Intermed Advisors, Inc. has 1 FDA 510(k) cleared medical devices. Based in Arlington, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Intermed Advisors, 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 - Intermed Advisors, Inc.
1 devices