Cardicare Company, Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Cardicare Company, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Aneroid Sphygmomanometer
2
Total
2
Cleared
0
Denied
Cardicare Company, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Hangzhou, Zhejiang, CN.
Last cleared in 2022. Active since 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardicare Company, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Irc as regulatory consultant.
FDA 510(k) Regulatory Record - Cardicare Company, Ltd.
2 devices