FDA 510(k) Applications Submitted by Shenzhen Mericonn Technology Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K212084 07/02/2021 Fetal Doppler Shenzhen Mericonn Technology Co., Ltd.
K212300 07/22/2021 Pulse Oximeter Shenzhen Mericonn Technology Co., Ltd.


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