Last synced on 25 January 2026 at 3:41 am

Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241120
510(k) Type
Traditional
Applicant
Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/24/2024
Days to Decision
62 days
Submission Type
Summary

Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241120
510(k) Type
Traditional
Applicant
Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/24/2024
Days to Decision
62 days
Submission Type
Summary