Class Class II

FAQ™ (102) (K240616)

K240616 2024-07-15 Traditional
Home/ Devices/ FAQ™ (102) (K240616)

Description

FAQ™ (102) by Foreo, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240616
Clearance Date2024-07-15
Clearance TypeTraditional
Product CodePAY
Regulation Number878.4420

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