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