K241120

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

510(k) number: K241120
Device name: Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S)
Applicant: Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd. CN
Product code: OHT — Light Based Over-The-Counter Hair Removal
Decision date: 2024-06-24
Date received: 2024-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Advisory committee: General, Plastic Surgery

Also available from FDA: K241120.pdf

Official FDA record: K241120

Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.