Class Class II

myLEDmask (K223147)

K223147 2023-05-14 Traditional
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Description

myLEDmask by Myblend — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223147
Clearance Date2023-05-14
Clearance TypeTraditional
Product CodeOHS
Regulation Number878.4810

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