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
FDA 510(k) Regulatory Record - Cardicare Company, Ltd. Cardiovascular ✕
2 devices