Cardicare Company, Ltd. is one of 2117 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, ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE MODEL HBPK-A
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.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Irc.
FDA 510(k) Regulatory Record - Cardicare Company, Ltd.
2 devices