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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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