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

FDA 510(k) Number Submission Date Device Name Applicant
K190207 02/04/2019 Blood Pressure Monitor Shenzhen Viatom Technology Co., Ltd.
K191088 04/24/2019 Checkme O2 Pulse Oximeter Shenzhen Viatom Technology Co., Ltd.
K193348 12/03/2019 Blood Pressure Monitor Shenzhen Viatom Technology Co., Ltd.
K203812 12/28/2020 Oxyfit Pulse Oximeter Shenzhen Viatom Technology Co., Ltd.


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