Last synced on 9 May 2025 at 11:05 pm

Hand-held IPL device (IPL Home Use Hair Removal Device) Model:FZ-608, FZ-608G, FZ-100, FZ-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221214
510(k) Type
Traditional
Applicant
Shenzhen IONKA Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/21/2022
Days to Decision
147 days
Submission Type
Summary

Hand-held IPL device (IPL Home Use Hair Removal Device) Model:FZ-608, FZ-608G, FZ-100, FZ-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221214
510(k) Type
Traditional
Applicant
Shenzhen IONKA Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/21/2022
Days to Decision
147 days
Submission Type
Summary