Medical Device Manufacturer · CN , Hangzhou, Zhejiang

Cardicare Company, Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008
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
1-2 of 2
Cleared Nov 28, 2022
Aneroid Sphygmomanometer
K222652 · DXQ
Cardiovascular · 88d
Cleared Sep 17, 2008
ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE MODEL HBPK-A
K082542 · DXQ
Cardiovascular · 14d
Filters
Filter by Specialty
All2 Cardiovascular 2