Last synced on 25 April 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
K230739
510(k) Type
Traditional
Applicant
Shenzhen IONKA Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/26/2023
Days to Decision
70 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
K230739
510(k) Type
Traditional
Applicant
Shenzhen IONKA Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/26/2023
Days to Decision
70 days
Submission Type
Summary