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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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