Class Class II

FoLix (K242349)

K242349 2024-09-09 Special
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Description

FoLix by Lumenis Be, Ltd. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242349
Clearance Date2024-09-09
Clearance TypeSpecial
Product CodeGEX
Regulation Number878.4810

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