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FDA Approved Machine Diode Laser 808nm

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FDA Approved Machine Diode Laser 808nm

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Re: K192516
Trade/Device Name: Diode Laser 808nm, Model: SL-HR10
Regulation Number: 21 CFR 878.4810
Regulation Name: Laser Surgical Instrument For Use In General And Plastic Surgery And In Dermatology
Regulatory Class: Class II
Product Code: GEX
Dated: September 10, 2019
Received: September 13, 2019
Keyword:
FDA
Diode Laser 808nm
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Beijing Super laser Technology Co., Ltd.

Beijing Super laser Technology Co., Ltd.

Beijing Superlaser Technology Co., Ltd

 

 

Professional  Aesthetics & Medical Laser Equipment Manufacturer. FDA/Medical CE/TUV / ISO13485 Approved. 14-Year Experience in OEM/ODM Service. 

2 floor,building3, No.2 zhongfu street, 

xihongmen town,daxing district,Beijing

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