Medaica, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Medaica, Inc. has 1 FDA 510(k) cleared medical devices. Based in Henderson, US.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medaica, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medaica, Inc.
1 devices