FDA 510(k) Applications Submitted by Dongguan kangweile Electronic Technology Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K230642 03/08/2023 Electronic Blood Pressure Monitor Dongguan kangweile Electronic Technology Co., Ltd.
K212171 07/12/2021 Electronic Blood Pressure Monitor Dongguan Kangweile Electronic Technology Co., Ltd.


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