Cardicare Company, Ltd.

Cardicare Company, Ltd. holds 2 FDA 510(k) medical device clearances, first cleared 2008, most recent 2022.

Top product codes for Cardicare Company, Ltd.

DXQ — Cardiovascular2 devices

Recent clearances by Cardicare Company, Ltd.

K222652 — Aneroid Sphygmomanometer; Single Patient Use Aneroid SphygmomanometerCode DXQ·2022-11-28
K082542 — ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE MODEL HBPK-ACode DXQ·2008-09-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.