FDA 510(k) Applications Submitted by CARDICARE COMPANY, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K082542 | 09/03/2008 | ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE MODEL HBPK-A | CARDICARE COMPANY, LTD. |
| K222652 | 09/01/2022 | Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer | Cardicare Company, Ltd. |
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