Class Class II

Painless IPL System – KDT750 (K220214)

K220214 2023-02-18 Traditional
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Description

Painless IPL System - KDT750 by Shanghai Omni Laser Skinology Co., Ltd. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220214
Clearance Date2023-02-18
Clearance TypeTraditional
Product CodeONF
Regulation Number878.4810

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