Class Class II

Q-Rejuvalight Pro Facewear (Model: P19-0023) (K230042)

K230042 2023-04-28 Traditional
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Description

Q-Rejuvalight Pro Facewear (Model: P19-0023) by Light Tree Ventures Europe B.V. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230042
Clearance Date2023-04-28
Clearance TypeTraditional
Product CodeOHS
Regulation Number878.4810

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