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

FDA 510(k) Number Submission Date Device Name Applicant
K173123 09/29/2017 Pulse Oximeter Shenzhen IMDK Medical Technology Co., Ltd.
K180419 02/15/2018 Ultrasonic Doppler (Model YM-2T8) Shenzhen IMDK Medical Technology Co., Ltd.
K221979 07/05/2022 Pulse Oximeter (Model C101A2, C101B1, C101A3) Shenzhen IMDK Medical Technology CO., Ltd.


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