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Shenzhen Wisonic Medical Technology Co. , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K230066Carnation series Diagnostic Ultrasound SystemSeptember 15, 2023
K211886Clivia series Diagnostic Ultrasound SystemDecember 2, 2021
K210154Labat series Diagnostic Ultrasound SystemJuly 30, 2021
K191347Paragon XHD Diagnostic Ultrasound SystemFebruary 7, 2020
K182715Piloter Exp/Piloter/Piloter P Diagnostic Ultrasound SystemNovember 20, 2018
K180461Navi e/Navi s/Navi X Diagnostic Ultrasound SystemMay 9, 2018
K163712Clover 50/Clover60/Clover70 Diagnostic Ultrasound SystemJanuary 2, 2018