Curatia Medical Co. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Curatia Medical Co. has 2 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Last cleared in 2022. Active since 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Curatia Medical Co. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Prime Path Medtech as regulatory consultant.
FDA 510(k) Regulatory Record - Curatia Medical Co.
2 devices