Class Class II

Diode Laser Therapy Device (DF-DIODE LASER-S1) (K241547)

K241547 2024-08-13 Traditional
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Description

Diode Laser Therapy Device (DF-DIODE LASER-S1) by Weifang Dragonfly Electronics Technology Co., Ltd. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241547
Clearance Date2024-08-13
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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