Class Class II

Thulium Laser System (Deluxlase) (K251919)

K251919 2025-09-26 Traditional
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Description

Thulium Laser System (Deluxlase) by Nanjing Bestview Laser S&T Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251919
Clearance Date2025-09-26
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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