Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S)— 510(k) K241120

Substantially Equivalent

Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd.

FDA 510(k) clearance K241120 for Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S), Substantially Equivalent on 2024-06-24. Applicant: Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd.. Device class: 2.

Clearance details

Applicant
Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd.
Product code
Code OHT
Device class
Class 2
Regulation
21 CFR 878.4810
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Dongguan, CN
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