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Cardicare Company, Ltd.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K222652 Aneroid Sphygmomanometer; Single Patient Use Aneroid SphygmomanometerDXQ2022-11-28 View
510(k) K082542 ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE MODEL HBPK-ADXQ2008-09-17 View
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