Embolization, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Embolization, Inc. has 1 FDA 510(k) cleared medical devices. Based in Boulder, US.
Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Embolization, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Boulder Biomed, LLC, Dba Boulder IQ Dba Boulder as regulatory consultant.
1 devices