FDA 510(k) Applications Submitted by Zhejiang LuDe Technology Development Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221857 | 06/27/2022 | Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201 | Zhejiang LuDe Technology Development Co., Ltd. |
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