FDA 510(k) Applications Submitted by Famidoc Technology Company Limited
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222887 | 09/23/2022 | Arm Blood Pressure Monitor/Automatic Wireless Smart Blood Pressure Monitor | Famidoc Technology Company Limited |
| K191673 | 06/24/2019 | Upper Arm Blood Pressure Monitor | Famidoc Technology Company Limited |
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