强脉冲光治疗装置（FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S）
K号: K241120 · 2024-06-24
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器械摘要
常见问题
What is the Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S)?
Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S) is a medical device that received FDA 510(k) clearance on 2024-06-24. The listed applicant is Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd.. The 510(k) number is K241120.
When did Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S) receive FDA 510(k) clearance?
Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S) received FDA 510(k) clearance on 2024-06-24, under 510(k) number K241120.
Who is the listed applicant for Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S)?
The FDA 510(k) record lists Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S)?
The FDA product code for Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S) is OHT.
相关临床试验
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相关器械（代码：OHT）
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官方来源
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