# Cardicare Company, Ltd.

- Location (FDA's records): Hangzhou City, CN
- FDA decisions: 2 (2008–2022): 2 510(k) clearances
- Product codes: DXQ (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Shanghai Caremate Medical Device Co., Ltd.: 1 (https://510kreport.com/company/shanghai-caremate-medical-device)

## Its most-cited devices
- K082542: Aneroid Sphygmomanometer with Stethoscope Model HBPK-a (2008), cited by 1

## Recent decisions
- K222652: Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer (Nov 28, 2022)
- K082542: Aneroid Sphygmomanometer with Stethoscope Model HBPK-a (Sep 17, 2008)

Source page: https://510kreport.com/company/cardicare