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

FDA 510(k) Number Submission Date Device Name Applicant
K230739 03/17/2023 Hand-held IPL device (IPL Home Use Hair Removal Device), Model: FZ-608, FZ-608G, FZ-100, FZ-200 Shenzhen IONKA Medical Technology Co., Ltd.
K221214 04/27/2022 Hand-held IPL device (IPL Home Use Hair Removal Device) Model:FZ-608, FZ-608G, FZ-100, FZ-200 Shenzhen IONKA Medical Technology Co., Ltd.


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