Class Class II

LeafPure-Echo (LM-LPNdA) (K253219)

K253219 2025-11-25 Traditional
Home/ Devices/ LeafPure-Echo (LM-LPNdA) (K253219)

Description

LeafPure-Echo (LM-LPNdA) by Shenzhen Leaflife Technology Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253219
Clearance Date2025-11-25
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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