Icentia, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Icentia, Inc. has 1 FDA 510(k) cleared medical devices. Based in Quebec, CA.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Icentia, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ultra Life Science Solutions, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Icentia, Inc.
1 devices